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Nodes: 2647,
Authors: 5321,
Journals: 428,
Outer References: 16458,
Words: 3536
Collection span: 1967 - 2005
View: Overview. Sorted by journal name.
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| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 301 | 0 | 0 | 1944 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):25-25 Crawford DC; Wilson B; Sherman SL Factors involved in the initial mutation of the fragile X CGG repeat as determined by sperm small pool-PCR. | 0 | 0 |
| 302 | 0 | 0 | 1945 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):26-26 Hagerman RJ; Tassone F; Leehey M; Hills J; Wilson R; et al. Cerebellar tremor and cerebellar cortical atrophy in older males with the fragile X premutation. | 0 | 0 |
| 303 | 0 | 0 | 1946 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):50-50 Neri G; Pomponi MG; Pietrobono R; Chiurazzi P; Oostra BA Differential reactivation of the FMR1 gene in fragile X patients cell lines. | 0 | 0 |
| 304 | 0 | 0 | 1947 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):50-50 Kenneson A; Zhang F; Warren ST Fragile X premutation alleles are associated with reduced FMRP levels due to a reduction of message translatability. | 0 | 0 |
| 305 | 0 | 0 | 1948 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):57-57 Li MM; Nelson L; Bamshad M; Ward K Fragile X mosaics in a family with multiple mildly affected individuals. | 0 | 0 |
| 306 | 0 | 0 | 1949 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):130-130 Khalifa M; Struthers J High frequency of Klinefelter syndrome among a large population of patients referred for Fragile X syndrome testing due to undiagnosed mental retardation. | 0 | 0 |
| 307 | 0 | 0 | 1950 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):135-135 Harris SW; Brown KE; Hills JL; Tassone F; Hagerman PJ; et al. Adaptive functioning and molecular relationships in individuals with fragile X syndrome. | 0 | 0 |
| 308 | 0 | 0 | 1951 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):184-184 Tassone F; Hagerman RJ; Taylor AK; Hagerman PJ Clinical and molecular correlations in individuals with a fragile X full mutation. | 0 | 0 |
| 309 | 0 | 0 | 1952 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):200-200 Ceman SS; Kenneson A; Nelson R; Jin C; Lakkis L; et al. Development and characterization of a unique set of anti-FMRP antibodies using a novel strategy. | 0 | 0 |
| 310 | 0 | 0 | 1953 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):236-236 Mathews DJ; Hudson R; Eichier E; Chakravarti A Sequence variation and linkage disequilibrium at the fragile X syndrome locus. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 311 | 0 | 0 | 1954 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):238-238 Sullivan AK; Crawford DC; Meadows KL; Wilson B; Sherman SL Parent-child transmission of intermediate FMR1 CGG repeat alleles: Examination of factors associated with repeat instability. | 0 | 0 |
| 312 | 0 | 0 | 1955 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):247-247 Brown NM; Friez MJ; Longshore JW; Stenzel TT Evaluation of an automated commercially available PCR kit for determination of Fragile X (FRAXA) normal, gray-zone and premutation allele sizes. | 0 | 0 |
| 313 | 0 | 0 | 1956 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):248-248 Murphy KM; Nunes ME Comparison of child-only versus mother/child sample collection in Fragile X testing. | 0 | 0 |
| 314 | 0 | 0 | 1957 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):254-254 Weinhaeusel A; Skarits C; Haas OA Methylation-sensitive PCR (MS-PCR) analysis of the fragile X (FRAXA) syndrome. | 0 | 0 |
| 315 | 0 | 0 | 1958 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):348-348 Dyack S; Steele L; Koultchitski G; Yang Y; Weksberg R; et al. AGG interruptions in the CGG trinucleotide repeat tract of the FMR1 gene may contribute to stability of Fragile X premutations. | 0 | 0 |
| 316 | 0 | 0 | 1959 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):360-360 Ramos FJ; Mila M; Ortilles M; Rife M; Tazon B; et al. Validity of the analysis of the FMRP expression in bloodsmears as a screening method for the Fragile X Syndrome. | 1 | 1 |
| 317 | 0 | 0 | 1960 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):364-364 Chen SH; Xu B; Shoof JM; Buroker NE; Scott CR Evidence for a stepwise expansion of the CGG repeats within the FMR1 gene. | 0 | 0 |
| 318 | 0 | 0 | 1961 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):365-365 Nolin SL; Rousseau F; Houck GE; Gargano AD; Biancalana V; et al. FMR1 CGG expansion to full mutation: What is the lower limit in premutation females? | 0 | 0 |
| 319 | 0 | 0 | 1962 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):365-365 O'Donnell WT; Warren ST Investigating the cause of macroorchidism in fragile X syndrome using oligonucleotide microarrays. | 0 | 0 |
| 320 | 0 | 0 | 1963 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):366-366 Raca G; Siyanova E; Mirkin S Janus effects of premutation size CGG repeats on gene expression. | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 321 | 0 | 0 | 1964 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):366-366 Parades WJ; Warren ST Meiotic stability of a fragile X premutation CGG trinucleotide repeat in a mouse model. | 0 | 0 |
| 322 | 0 | 0 | 1965 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):415-415 Najmabadi H; Taghizadeh F; Teimourian SH; Karimi-Nejad R; Shafeghati Y; et al. Molecular analysis of Fragile X syndrome in Iranian population. | 0 | 0 |
| 323 | 0 | 0 | 1966 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):428-428 Brown WT; Ding X; Idrissi AE; Scalia J; Glicksman A; et al. Fragile X transgene and embryonic lethality in mice. | 0 | 0 |
| 324 | 29 | 40 | 2094 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(2):351-360 Toledano-Alhadef H; Basel-Vanagaite L; Magal N; Davidov B; Ehrlich S; et al. Fragile-X carrier screening and the prevalence of premutation and full-mutation carriers in Israel | 13 | 22 |
| 325 | 21 | 34 | 2095 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(3):504-515 Wohrle D; Salat U; Hameister H; Vogel W; Steinbach P Demethylation, reactivation, and destabilization of human fragile X full-mutation alleles in mouse embryocarcinoma cells | 4 | 10 |
| 326 | 0 | 0 | 2096 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):177-177 Hagerman RJ; Greco C; Chudley A; Leehey M; Tassone F; et al. Neuropathology and neurodegenerative features in some older male premutation carriers of fragile X syndrome. | 3 | 4 |
| 327 | 0 | 0 | 2097 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):291-291 Thiele H; Peters H; Bahrke D; Hansmann I Homozygosity for a premutation of the FMR1 gene and normal phenotype in two sisters from a family with fragile X syndrome. | 0 | 0 |
| 328 | 0 | 0 | 2098 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):352-352 Gantois I; Reyniers E; Kooy RF Identification of genes differentially expressed in the fragile X syndrome. | 0 | 0 |
| 329 | 0 | 0 | 2099 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):372-372 Naumann F; Muller-Hartmann H; Deissler H; Doerfler W Functional studies on the human 5 '-CGG-3 '-binding protein CGGBP1 (p20). | 0 | 0 |
| 330 | 0 | 0 | 2100 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):372-372 Neri G; Pomponi MG; Pietrobono R; Chiurazzi P Pharmacological reactivation of the FMR1 gene of the fragile X syndrome. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 331 | 0 | 0 | 2101 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):430-430 Jakupciak JP; O'Connell CD; Atha DA; Richie KL Standardization of PCR amplification for fragile X trinucleotide repeat measurements. | 0 | 0 |
| 332 | 0 | 0 | 2102 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):431-431 Jenkins EC; Li SY; Yao XL; Lanter S; Sudhalter V; et al. Detecting mosaic FMR-1 (fragile X) mutations: Southern blotting versus monoclonal antibody analysis. | 0 | 0 |
| 333 | 0 | 0 | 2103 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):436-436 Patel ZM; Menon SR; D'souza AK; Adhia RA; Sanghavi DA; et al. Validity of the analysis of FMRP expression in blood smears as a screening method for the fragile X syndrome in Indian population. | 0 | 0 |
| 334 | 0 | 0 | 2104 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):438-438 Zhou Y; Chong SS Simplified molecular diagnostic testing for fragile X syndrome using methylation-specific PCR (ms-PCR). | 0 | 0 |
| 335 | 0 | 0 | 2105 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):554-554 Heine-Sur D; Pico G; Torres-Juan L; Bernues M; Iglesias J; et al. A female with Fragile-X shows an affected male-like phenotype and skewed inactivation of the functional chromosome. | 0 | 0 |
| 336 | 0 | 0 | 2106 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):585-585 Essop FB; Greenberg J; Basel D; Krause A Molecular analysis of a fragile X family with two females homozygous for a premutation. | 0 | 0 |
| 337 | 0 | 0 | 2107 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):586-586 Nolin SL; Houck GE; Gargano AD; Brown WT Large fragile X premutatin alleles may often contain two AGG Interruptions. | 0 | 0 |
| 338 | 0 | 0 | 2108 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):635-635 Dobkin CS; Ding X; Brown WT; El Idrissi A Reduced hippocampal GABAa receptors and increased kainic acid seizure susceptibility in the fragile X mouse. | 0 | 0 |
| 339 | 0 | 0 | 2109 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):667-667 Brown WT; Nolin S; Houck GE; Ding XH; Glicksman A; et al. The Fragile X Syndrome: Screening and prenatal diagnosis. | 0 | 0 |
| 340 | 0 | 0 | 2110 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):669-669 Mallolas J; Badenas C; Rite M; Soler A; Borrell A; et al. Prospective study of molecular fragile X syndrome prenatal diagnosis. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 341 | 0 | 0 | 2217 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):175-175 Jin P; Zhang F; Zarnescu DC; Moses K; Lucchesi JC; et al. A Drosophila model of fragile X premutation: CGG repeat instability and dominant-negative effects of premutation riboCGG repeat. | 0 | 0 |
| 342 | 0 | 0 | 2218 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):185-185 Jacquemont S; Hagerman RJ; Leehey M; Greco C; Brunberg J; et al. Characterization of a progressive neurological condition in older adult male carriers of the fragile X premutation. | 2 | 2 |
| 343 | 0 | 0 | 2219 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):259-259 Hagerman PJ; Greco CM; Hagerman RJ; Tassone F; Chudley AE; et al. Neuronal intranuclear inclusions in a tremor/ataxia syndrome among fragile X premutation carriers. | 0 | 0 |
| 344 | 0 | 0 | 2220 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):270-270 Griffin KJ; Bei T; Meck J; Wong LJ; Bondy C; et al. Gender ambiguity and fragile X: a new syndrome. | 0 | 0 |
| 345 | 0 | 0 | 2221 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):287-287 Hagerman R; Goodlin-Jones BL; Spence S; Albrect L; Bacalman S; et al. The fragile X premutation and autistic spectrum disorders. | 0 | 0 |
| 346 | 0 | 0 | 2222 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):288-288 Harris SW; Goodlin-Jones BL; Bacalman S; Jardini T; Rao S; et al. Fragile X and autism diagnosis by two standard methodologies. | 0 | 0 |
| 347 | 0 | 0 | 2223 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):331-331 Tassone F; Sahota P; Pleasant N; Laird C; Hagerman P Methylation analysis of the promoter region in fragile X males with hypermethylated, full mutation alleles | 0 | 0 |
| 348 | 0 | 0 | 2224 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):338-338 Naumann F; Schmitz B; Doerfler W Expression of the human and murine 5 '-(CGG)(n)-3 '-binding proteins CGGBP1. | 0 | 0 |
| 349 | 0 | 0 | 2225 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):347-347 Brown WT; Nolin SL; Dobkin CS; Houck GS; Glicksman A; et al. Frequency of fragile X in multiplex autism: Testing the AGRE families. | 0 | 0 |
| 350 | 0 | 0 | 2226 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):373-373 Ennis S; Brightwell G; Collins A; Jacobs P; Morton NE Phylogeny of fragile X haplotypes from an English population. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 351 | 0 | 0 | 2227 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):377-377 Zabala WM; Nava N; Gonzalez S; Delgado W; Borjas L; et al. Clinical and molecular analysis of the fragile X syndrome in mentally retarded males from the Venezuelan northwestern region. | 0 | 0 |
| 352 | 0 | 0 | 2228 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):384-384 Chen S; Schoof JM; Lemoine CJ; Gordon CL; Scott CR Prevalence survey of the Fragile X E syndrome referred for Fragile X syndrome testing in boys with mental retardation. | 0 | 0 |
| 353 | 0 | 0 | 2229 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):505-505 Dobkin CS; Ding XH; Houck GE; Mitchell E; Brown WT; et al. A rare Eag I polymorphism that may confound fragile X diagnosis. | 0 | 0 |
| 354 | 0 | 0 | 2230 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):507-507 Neri G; Tabolacci E; Pietrobono R; Pomponi MG; Chiurazzi P Histone hyperacetylation and reactivation of the fragile X syndrome gene. | 0 | 1 |
| 355 | 0 | 0 | 2231 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):518-518 Maranduba CMC; Vianna-Morgante AM; Passos-Bueno MR P172H mutation in the TM4SF2 gene accounts for 1% of non-fragile X mental retardation in Brazilian patients. | 0 | 0 |
| 356 | 0 | 0 | 2232 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):523-523 Bastaki LA; Al-Awadi SA; Hegazi FA; Turky NA; Mustafa MA; et al. PCR technique and significance in fragile X syndrome. | 0 | 0 |
| 357 | 10 | 37 | 2233 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):923-932 Coffee B; Zhang FP; Ceman S; Warren ST; Reines D Histone modifications depict an aberrantly heterochromatinized FMR1 gene in fragile X syndrome | 3 | 14 |
| 358 | 32 | 39 | 2348 2003 AMERICAN JOURNAL OF HUMAN GENETICS 72(2):454-464 Nolin SL; Brown WT; Glicksman A; Houck GE; Gargano AD; et al. Expansion of the fragile X CGG repeat in females with premutation or intermediate alleles | 13 | 21 |
| 359 | 19 | 36 | 2349 2003 AMERICAN JOURNAL OF HUMAN GENETICS 72(4):869-878 Jacquemont S; Hagerman RJ; Leehey M; Grigsby J; Zhang L; et al. Fragile X premutation tremor/ataxia syndrome: Molecular, clinical, and neuroimaging correlates | 26 | 44 |
| 360 | 0 | 0 | 2350 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):162-162 Jin P; Ceman S; Zarnescu DC; Nakamoto M; Mowrey J; et al. Biochemical and genetic interaction between the fragile X mental retardation protein and the microRNA pathway. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 361 | 0 | 0 | 2351 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):163-163 Allen E; Letz R; Sherman S Association of FMR1 CGG repeat size, X-inactivation ratio and transcript level with cognitive performance among women. | 0 | 0 |
| 362 | 0 | 0 | 2352 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):163-163 Cronister A; Teicher J; Custer T; Rohlfs EM Prevalence of premutation and intermediate alleles among patients referred for fragile X carrier testing. | 0 | 0 |
| 363 | 0 | 0 | 2353 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):163-163 Jiang Y; Wakui K; Liu Q; Kashork CD; Lehoczky J; et al. A fragile X mental retardation protein interacting protein maps to the proximal breakpoint of the Prader-Willi syndrome common deletion region. | 0 | 0 |
| 364 | 0 | 0 | 2354 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):163-163 Jacquemont S; Hagerman RJ; Leehey MA; Hall DA; Levine RA; et al. Penetrance of the fragile X-associated tremor/ataxia syndrome (FXTAS) in a premutation carrier population: Initial results from a California family-based study. | 0 | 0 |
| 365 | 0 | 0 | 2355 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):266-266 Hagerman RJ; Jacquemont S; Tassone F; Greco C; Brunberg J; et al. Fragile X-associated tremor/ataxia syndrome (FXTAS) involvement in females | 0 | 0 |
| 366 | 0 | 0 | 2356 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):296-296 Harris SW; Tassone F; Barbato I; Hagerman RJ FMRP, FMR1-mRNA, and psychopathology correlations in women with the fragile X premutation. | 0 | 0 |
| 367 | 0 | 0 | 2357 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):314-314 Medne L; Russell K; Ming J; Krantz ID; Souders M; et al. Subtelomeric FISH analysis in 108 autistic patients as adjunct to chromosome analysis and fragile X testing | 0 | 0 |
| 368 | 0 | 0 | 2358 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):330-330 Herman K; Nowicki S; Tassone F; Koldewyn K; Bacalman S; et al. Correlations between DNA, FMRP, and mRNA levels and ADOS-G and ADI-R scores in patients with Fragile X Syndrome. | 0 | 0 |
| 369 | 0 | 0 | 2359 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):337-337 Nolin SL; Houck GE; Glicksman A; Gargano AD; Brown WT Large fragile X premutation alleles may often contain two AGG interruptions. | 0 | 0 |
| 370 | 0 | 0 | 2360 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):348-348 Tabolacci E; Pietrobono R; Chiurazzi P; Neri G Variation of histone acetylation/methylation in the FMR1 gene of the fragile X syndrome following pharmacological reactivation. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 371 | 0 | 0 | 2361 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):348-348 O'Donnell WT; Ceman S; Warren ST Phosphorylation of the fragile X mental retardation protein regulates translation of its mRNA ligands. | 0 | 0 |
| 372 | 0 | 0 | 2362 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):372-372 Reddy K Autism: Incidence of cytogenetic abnormality and fragile-X syndrome. | 0 | 0 |
| 373 | 0 | 0 | 2363 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):377-377 Ennis S; Collins A; Morton NE The use of SNP-based haplotypes and LD blocks to positionally clone modifying determinants of expansion of the Fragile X triplet repeat | 0 | 0 |
| 374 | 0 | 0 | 2364 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):383-383 Rigby AS; Turk J; Mills AC; James N; Hollis C; et al. Social functioning in male premutation carriers of Fragile X (FRAX) syndrome | 0 | 0 |
| 375 | 0 | 0 | 2365 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):457-457 Mirakhory M; Aleyassin A Study of folic acid pathway genes alteration in fragile X syndrome. | 0 | 0 |
| 376 | 0 | 0 | 2366 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):555-555 Di Maria E; Grasso M; Pigullo S; Faravelli F; Abbruzzese G; et al. Further evidence that a tremor/ataxia syndrome may occur in Fragile X premutation carriers: findings from two clinical series. | 0 | 0 |
| 377 | 0 | 0 | 2367 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):557-557 Gantois I; Vandesompele J; Speleman F; D'Hooge R; Severijnen LA; et al. Expression profiling reveals involvement of the GABA(A) receptor subunit delta in the fragile X syndrome. | 0 | 0 |
| 378 | 0 | 0 | 2368 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):573-573 Wronska A; Ju W; Brown WT; Zhong N Studies of FMRP-binding RNAs with a yeast tri-hybrid system. | 0 | 0 |
| 379 | 0 | 0 | 2369 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):585-585 Fan H; Booker JK; McCandless SE; Shashi V; Farber RA Mosaicism for FMR1 gene full mutation and deletion in a fragile X female. | 0 | 0 |
| 380 | 0 | 0 | 2370 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):586-586 Greco CM; Tassone F; Jaquemont S; Hagerman RJ; Sahota PK; et al. Intranuclear neuronal inclusions in two female carriers of the fragile X premutation | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 381 | 0 | 0 | 2371 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):587-587 Tassone F; Hagerman RJ; Garcia D; Sahota PK; Khandjian EW; et al. Intranuclear inclusions in fragile X-associated tremor/ataxia syndrome neuronal cells from five premutation carriers. | 0 | 0 |
| 382 | 0 | 0 | 2372 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):589-589 Chen LS; Tassone F; Sahota P; Hagerman PJ The (CGG)(n) repeat elements within the 5 ' untranslated region of the FMR1 message provides both positive and negative cis effects on in vivo translation of a downstream reporter. | 0 | 0 |
| 383 | 41 | 80 | 2480 2004 AMERICAN JOURNAL OF HUMAN GENETICS 74(5):805-816 Hagerman PJ; Hagerman RJ The fragile-X premutation: A maturing perspective | 8 | 14 |
| 384 | 15 | 26 | 2481 2004 AMERICAN JOURNAL OF HUMAN GENETICS 74(5):1051-1056 Hagerman RJ; Leavitt BR; Farzin F; Jacquemont S; Greco CM; et al. Fragile-X-associated tremor/ataxia syndrome (FXTAS) in females with the FMR1 premutation | 3 | 7 |
| 385 | 1 | 1 | 2482 2004 AMERICAN JOURNAL OF HUMAN GENETICS 75(2):352-352 Hagerman; Hagerman The fragile-X premutation: A maturing perspective (vol 74, pg 805, 2003) | 0 | 0 |
| 386 | 2 | 10 | 2483 2004 AMERICAN JOURNAL OF HUMAN GENETICS 75(4):730-731 Mandel JL Comparative frequency of fragile-X (FMR1) and creatine transporter (SLC6A8) mutations in X-linked mental retardation | 1 | 1 |
| 387 | 1 | 5 | 2484 2004 AMERICAN JOURNAL OF HUMAN GENETICS 75(4):731-732 Salomons GS; Ropers HH Comparative frequency of fragile-X (FMR1) and creatine transporter (SLC6A8) mutations in X-linked mental retardation - Reply | 0 | 0 |
| 388 | 18 | 41 | 2620 2005 AMERICAN JOURNAL OF HUMAN GENETICS 76(2):302-311 Edamura KN; Leonard MR; Pearson CE Role of replication and CpG methylation in fragile X syndrome CGG deletions in primate cells | 0 | 0 |
| 389 | 0 | 6 | 6 1980 AMERICAN JOURNAL OF MEDICAL GENETICS 7(4):503-505 KAISERMCCAW B; HECHT F; CADIEN JD; MOORE BC FRAGILE X-LINKED MENTAL-RETARDATION | 14 | 22 |
| 390 | 0 | 0 | 50 1982 AMERICAN JOURNAL OF MEDICAL GENETICS 11(4):489-495 HECHT F; JACKY PB; SUTHERLAND GR THE FRAGILE X-CHROMOSOME - CURRENT METHODS | 16 | 35 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 391 | 1 | 20 | 51 1982 AMERICAN JOURNAL OF MEDICAL GENETICS 13(2):139-148 BROOKWELL R; DANIEL A; TURNER G; FISHBURN J THE FRAGILE X(Q27) FORM OF X-LINKED MENTAL-RETARDATION - FUDR AS AN INDUCING AGENT FOR FRA(X)(Q27) EXPRESSION IN LYMPHOCYTES, FIBROBLASTS, AND AMNIOCYTES | 24 | 49 |
| 392 | 8 | 32 | 108 1983 AMERICAN JOURNAL OF MEDICAL GENETICS 14(4):699-712 CHUDLEY AE; KNOLL J; GERRARD JW; SHEPEL L; MCGAHEY E; et al. FRAGILE (X) X-LINKED MENTAL-RETARDATION .1. RELATIONSHIP BETWEEN AGE AND INTELLIGENCE AND THE FREQUENCY OF EXPRESSION OF FRAGILE (X)(Q28) | 56 | 80 |
| 393 | 4 | 5 | 109 1983 AMERICAN JOURNAL OF MEDICAL GENETICS 14(4):795-796 DAKER MG FRAGILE X-CHROMOSOME IN NORMAL MALES | 2 | 4 |
| 394 | 1 | 1 | 110 1983 AMERICAN JOURNAL OF MEDICAL GENETICS 14(4):797-797 HECHT F; JACKY PB; SUTHERLAND GR FRAGILE X-CHROMOSOME IN NORMAL MALES - REPLY | 1 | 2 |
| 395 | 2 | 28 | 111 1983 AMERICAN JOURNAL OF MEDICAL GENETICS 15(1):113-119 FILIPPI G; RINALDI A; ARCHIDIACONO N; ROCCHI M; BALAZS I; et al. LINKAGE BETWEEN G6PD AND FRAGILE-X SYNDROME | 19 | 43 |
| 396 | 1 | 14 | 112 1983 AMERICAN JOURNAL OF MEDICAL GENETICS 15(4):631-635 HOWARDPEEBLES PN; FINLEY WH SCREENING OF MENTALLY-RETARDED MALES FOR MACRO-ORCHIDISM AND THE FRAGILE-X CHROMOSOME | 16 | 22 |
| 397 | 103 | 406 | 172 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):5-94 OPITZ JM; SUTHERLAND GR CONFERENCE REPORT - INTERNATIONAL WORKSHOP ON THE FRAGILE-X AND X-LINKED MENTAL-RETARDATION | 52 | 116 |
| 398 | 4 | 16 | 173 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):111-121 HAGERMAN RJ; VANHOUSEN K; SMITH ACM; MCGAVRAN L CONSIDERATION OF CONNECTIVE-TISSUE DYSFUNCTION IN THE FRAGILE-X SYNDROME | 25 | 35 |
| 399 | 1 | 12 | 174 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):123-131 HAGERMAN RJ; SYNHORST DP MITRAL-VALVE PROLAPSE AND AORTIC DILATATION IN THE FRAGILE-X SYNDROME | 9 | 17 |
| 400 | 2 | 16 | 175 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):159-174 MERYASH DL; CRONK CE; SACHS B; GERALD PS AN ANTHROPOMETRIC STUDY OF MALES WITH THE FRAGILE-X SYNDROME | 26 | 43 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 401 | 4 | 29 | 176 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):175-194 PARTINGTON MW THE FRAGILE-X SYNDROME .2. PRELIMINARY DATA ON GROWTH AND DEVELOPMENT IN MALES | 52 | 65 |
| 402 | 3 | 25 | 177 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):195-207 SIMPSON NE; NEWMAN BJ; PARTINGTON MW FRAGILE-X SYNDROME .3. DERMATOGLYPHIC STUDIES IN MALES | 10 | 16 |
| 403 | 0 | 4 | 178 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):209-214 RHOADS FA FRAGILE-X SYNDROME IN HAWAII - A SUMMARY OF CLINICAL-EXPERIENCE | 12 | 21 |
| 404 | 10 | 43 | 179 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):215-239 JENKINS EC; BROWN WT; BROOKS J; DUNCAN CJ; RUDELLI RD; et al. EXPERIENCE WITH PRENATAL FRAGILE-X DETECTION | 35 | 44 |
| 405 | 4 | 16 | 180 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):241-252 SOUDEK D; PARTINGTON MW; LAWSON JS THE FRAGILE-X SYNDROME .1. FAMILIAL VARIATION IN THE PROPORTION OF LYMPHOCYTES WITH THE FRAGILE SITE IN MALES | 24 | 29 |
| 406 | 0 | 2 | 181 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):253-254 DEV VG; MIXON C 5-AZACYTIDINE DECREASES THE FREQUENCY OF FRAGILE-X EXPRESSION IN PERIPHERAL LYMPHOCYTE CULTURE | 4 | 6 |
| 407 | 2 | 11 | 182 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):255-257 DANIEL A; EKBLOM L; PHILLIPS S FRAGILE-X EXPRESSION SUPPRESSED IN EITHER FUDR OR METHOTREXATE TREATED FIBROBLASTS BY PRETREATMENT WITH 5-AZACYTIDINE | 3 | 5 |
| 408 | 3 | 20 | 183 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):259-273 HOLDEN JJA; WANG HS; WHITE BN THE FRAGILE-X SYNDROME .4. PROGRESS TOWARDS THE IDENTIFICATION OF LINKED RESTRICTION FRAGMENT LENGTH VARIANTS (RFLVS) | 4 | 13 |
| 409 | 1 | 2 | 184 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):275-276 HOWARDPEEBLES PN; CARROLL AJ RECOMBINATION BETWEEN THE FRAGILE-X AND G6PD | 1 | 3 |
| 410 | 6 | 13 | 185 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):289-297 BROWN WT; JENKINS EC; FRIEDMAN E; BROOKS J; COHEN IL; et al. FOLIC-ACID THERAPY IN THE FRAGILE-X SYNDROME | 20 | 28 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 411 | 3 | 9 | 186 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):299-301 ERBE RW FOLIC-ACID THERAPY IN THE FRAGILE-X SYNDROME | 4 | 8 |
| 412 | 2 | 11 | 187 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):303-310 WANG JCC; ERBE RW FOLATE METABOLISM IN CELLS FROM FRAGILE-X SYNDROME PATIENTS AND CARRIERS | 15 | 22 |
| 413 | 8 | 12 | 188 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(4):853-855 GARDNER RJM FRAGILE-X MALES WITH NORMAL INTELLIGENCE - AND IF SO, WHY | 4 | 7 |
| 414 | 0 | 2 | 189 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(4):857-858 CHUDLEY AE; KNOLL JH; GERRARD JW FRAGILE-X MALES WITH NORMAL INTELLIGENCE - AND IF SO, WHY - REPLY | 0 | 0 |
| 415 | 4 | 13 | 190 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 18(3):483-491 DANIEL A; EKBLOM L; PHILLIPS S CONSTITUTIVE FRAGILE SITES 1P31, 3P14, 6Q26, AND 16Q23 AND THEIR USE AS CONTROLS FOR FALSE-NEGATIVE RESULTS WITH THE FRAGILE(X) | 12 | 50 |
| 416 | 1 | 12 | 248 1985 AMERICAN JOURNAL OF MEDICAL GENETICS 21(4):691-696 WANG JCC; BEARDSLEY GP; ERBE RW ANTIFOLATE-INDUCED MISINCORPORATION OF DEOXYURIDINE MONOPHOSPHATE INTO DNA BY CELLS FROM PATIENTS WITH THE FRAGILE-X SYNDROME | 2 | 5 |
| 417 | 12 | 32 | 249 1985 AMERICAN JOURNAL OF MEDICAL GENETICS 21(4):709-717 PEMBREY ME; WINTER RM; DAVIES KE A PRE-MUTATION THAT GENERATES A DEFECT AT CROSSING OVER EXPLAINS THE INHERITANCE OF FRAGILE X MENTAL RETARDATION | 82 | 116 |
| 418 | 4 | 12 | 250 1985 AMERICAN JOURNAL OF MEDICAL GENETICS 21(4):771-775 SHIMANUKI K; LIN MS; WILSON MG REDUCTION OF FRAGILE X-EXPRESSION IN BLOOD AFTER CRYOPRESERVATION | 1 | 3 |
| 419 | 7 | 13 | 251 1985 AMERICAN JOURNAL OF MEDICAL GENETICS 22(2):415-416 BARBI G; STEINBACH P FRAGILE-X AND MARTIN-BELL SYNDROME - NEW SOURCE OF INFORMATION | 1 | 3 |
| 420 | 7 | 19 | 252 1985 AMERICAN JOURNAL OF MEDICAL GENETICS 22(3):571-575 MITCHELL JA; WRAY J; MICHALSKI K NEUROFIBROMATOSIS AND FRAGILE-X SYNDROME IN THE SAME PATIENT | 2 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 421 | 1 | 2 | 320 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):11-67 TURNER G; OPITZ JM; BROWN WT; DAVIES KE; JACOBS PA; et al. CONFERENCE REPORT - 2ND INTERNATIONAL WORKSHOP ON THE FRAGILE-X AND ON X-LINKED MENTAL-RETARDATION | 51 | 71 |
| 422 | 8 | 18 | 321 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):111-126 PARTINGTON MW FEMALE RELATIVES IN FAMILIES WITH THE FRAGILE X-SYNDROME | 4 | 7 |
| 423 | 5 | 26 | 322 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):157-169 FRYNS JP THE FEMALE AND THE FRAGILE-X - A STUDY OF 144 OBLIGATE FEMALE CARRIERS | 78 | 103 |
| 424 | 5 | 11 | 323 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):171-178 SIMPSON NE DERMATOGLYPHIC INDEXES OF MALES WITH THE FRAGILE-X SYNDROME AND OF THE FEMALE HETEROZYGOTES | 6 | 10 |
| 425 | 2 | 8 | 324 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):179-187 SHELLHART WC; CASAMASSIMO PS; HAGERMAN RJ; BELANGER GK ORAL FINDINGS IN FRAGILE-X SYNDROME | 4 | 8 |
| 426 | 3 | 18 | 325 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):189-194 LOEHR JP; SYNHORST DP; WOLFE RR; HAGERMAN RJ AORTIC ROOT DILATATION AND MITRAL-VALVE PROLAPSE IN THE FRAGILE-X SYNDROME | 19 | 28 |
| 427 | 4 | 27 | 326 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):195-206 HANSON DM; JACKSON AW; HAGERMAN RJ SPEECH DISTURBANCES (CLUTTERING) IN MILDLY IMPAIRED MALES WITH THE MARTIN-BELL FRAGILE-X SYNDROME | 40 | 46 |
| 428 | 4 | 11 | 327 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):207-211 WILLIAMS CA; CANTU ES; FRIAS JL BRIEF CLINICAL REPORT - METAPHYSEAL DYSOSTOSIS AND CONGENITAL NYSTAGMUS IN A MALE INFANT WITH THE FRAGILE-X SYNDROME | 2 | 6 |
| 429 | 2 | 17 | 328 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):227-239 BERKOVITZ GD; WILSON DP; CARPENTER NJ; BROWN TR; MIGEON CJ GONADAL-FUNCTION IN MEN WITH THE MARTIN-BELL (FRAGILE-X) SYNDROME | 10 | 14 |
| 430 | 11 | 38 | 329 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):241-262 HAGERMAN RJ; JACKSON AW; LEVITAS A; BRADEN M; MCBOGG P; et al. ORAL FOLIC-ACID VERSUS PLACEBO IN THE TREATMENT OF MALES WITH THE FRAGILE-X SYNDROME | 19 | 27 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 431 | 9 | 17 | 330 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):263-271 BROWN WT; COHEN IL; FISCH GS; WOLFSCHEIN EG; JENKINS VA; et al. HIGH-DOSE FOLIC-ACID TREATMENT OF FRAGILE-(X) MALES | 9 | 14 |
| 432 | 9 | 27 | 331 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):273-289 FROSTERISKENIUS U; BODEKER K; OEPEN T; MATTHES R; PIPER U; et al. FOLIC-ACID TREATMENT IN MALES AND FEMALES WITH FRAGILE-(X)-SYNDROME | 10 | 15 |
| 433 | 6 | 12 | 332 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):291-296 WELLS TE; MADISON LS ASSESSMENT OF BEHAVIOR-CHANGE IN A FRAGILE-X SYNDROME MALE TREATED WITH FOLIC-ACID | 3 | 5 |
| 434 | 17 | 42 | 333 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):297-311 JENKINS EC; BROWN WT; WILSON MG; LIN MS; ALFI OS; et al. THE PRENATAL DETECTION OF THE FRAGILE-X CHROMOSOME - REVIEW OF RECENT EXPERIENCE | 17 | 27 |
| 435 | 21 | 26 | 334 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):313-324 TOMMERUP N; AULA P; GUSTAVII B; HEIBERG A; HOLMGREN G; et al. 2ND TRIMESTER PRENATAL-DIAGNOSIS OF THE FRAGILE-X | 7 | 14 |
| 436 | 18 | 51 | 335 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):341-352 BROWN WT; JENKINS EC; COHEN IL; FISCH GS; WOLFSCHEIN EG; et al. FRAGILE-X AND AUTISM - A MULTICENTER SURVEY | 72 | 110 |
| 437 | 8 | 25 | 336 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):353-358 MCGILLIVRAY BC; HERBST DS; DILL FJ; SANDERCOCK HJ; TISCHLER B INFANTILE-AUTISM - AN OCCASIONAL MANIFESTATION OF FRAGILE-(X) MENTAL-RETARDATION | 19 | 28 |
| 438 | 13 | 42 | 337 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):359-374 HAGERMAN RJ; JACKSON AW; LEVITAS A; RIMLAND B; BRADEN M AN ANALYSIS OF AUTISM IN 50 MALES WITH THE FRAGILE-X SYNDROME | 79 | 109 |
| 439 | 15 | 32 | 338 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):375-380 HAGERMAN RJ; CHUDLEY AE; KNOLL JH; JACKSON AW; KEMPER M; et al. AUTISM IN FRAGILE-X FEMALES | 32 | 46 |
| 440 | 4 | 12 | 339 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):393-401 REISS AL; FEINSTEIN C; TOOMEY KE; GOLDSMITH B; ROSENBAUM K; et al. PSYCHIATRIC DISABILITY ASSOCIATED WITH THE FRAGILE-X CHROMOSOME | 30 | 45 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 441 | 6 | 18 | 340 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):403-408 WAHLSTROM J; GILLBERG C; GUSTAVSON KH; HOLMGREN G INFANTILE-AUTISM AND THE FRAGILE-X - A SWEDISH MULTICENTER STUDY | 23 | 44 |
| 442 | 7 | 13 | 341 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):429-443 LEDBETTER DH; AIRHART SD; NUSSBAUM RL SOMATIC-CELL HYBRID STUDIES OF FRAGILE-(X) EXPRESSION IN A CARRIER FEMALE AND TRANSMITTING MALE | 10 | 18 |
| 443 | 1 | 14 | 342 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):445-455 LEDBETTER DH; AIRHART SD; NUSSBAUM RL CAFFEINE ENHANCES FRAGILE-(X) EXPRESSION IN SOMATIC-CELL HYBRIDS | 5 | 18 |
| 444 | 8 | 16 | 343 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):467-473 KRAWCZUN MS; LELE KP; JENKINS EC; BROWN WT FRAGILE-X EXPRESSION INCREASED BY LOW CELL-CULTURE DENSITY | 5 | 8 |
| 445 | 5 | 16 | 344 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):475-481 JENKINS EC; KASTIN BR; KRAWCZUN MS; LELE KP; SILVERMAN WP; et al. FRAGILE-X CHROMOSOME FREQUENCY IS CONSISTENT TEMPORALLY AND WITHIN REPLICATE CULTURES | 2 | 3 |
| 446 | 5 | 11 | 345 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):511-514 HOWARDPEEBLES PN METHIONINE METABOLISM AND FRAGILE-X EXPRESSION | 0 | 4 |
| 447 | 4 | 4 | 346 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):527-530 TOMMERUP N; HOLMGREN G; STEINBACH P FRAGILE-X - CARRIER DETECTION IN PREGNANCY | 1 | 4 |
| 448 | 3 | 7 | 347 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):531-535 JENKINS EC; DUNCAN CJ; KRAWCZUN MS; BERNS LM; SANZ MM; et al. FREQUENCY OF TRIRADIAL OR MULTIRADIAL CONFIGURATIONS IN FRAGILE-X IDENTIFICATION | 3 | 5 |
| 449 | 4 | 18 | 348 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):537-544 NIELSEN KB SEX-CHROMOSOME ANEUPLOIDY IN FRAGILE-X CARRIERS | 1 | 6 |
| 450 | 0 | 5 | 349 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):557-562 UCHIDA IA; FREEMAN VCP; BASRUR PK THE FRAGILE-X IN CATTLE | 6 | 20 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 451 | 1 | 3 | 350 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):567-572 JACOBS PA; MAYER M; ABRUZZO MA STUDIES OF THE FRAGILE (X) SYNDROME IN POPULATIONS OF MENTALLY-RETARDED INDIVIDUALS IN HAWAII | 13 | 16 |
| 452 | 1 | 10 | 351 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):581-587 GUSTAVSON KH; BLOMQUIST H; HOLMGREN G PREVALENCE OF THE FRAGILE-X SYNDROME IN MENTALLY-RETARDED BOYS IN A SWEDISH COUNTY | 53 | 75 |
| 453 | 4 | 11 | 352 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):589-595 SANFILIPPO S; RAGUSA RM; MUSUMECI S; NERI G FRAGILE-X MENTAL-RETARDATION - PREVALENCE IN A GROUP OF INSTITUTIONALIZED PATIENTS IN ITALY AND DESCRIPTION OF A NOVEL EEG PATTERN | 15 | 22 |
| 454 | 2 | 6 | 353 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):611-617 JACOBS PA; SHERMAN S; TURNER G; WEBB T THE FRAGILE(X) SYNDROME - THE MUTATION PROBLEM | 14 | 19 |
| 455 | 6 | 15 | 354 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):643-664 BROWN WT; GROSS AC; CHAN CB; JENKINS EC DNA LINKAGE STUDIES IN THE FRAGILE-X SYNDROME SUGGEST GENETIC-HETEROGENEITY | 36 | 49 |
| 456 | 3 | 23 | 355 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):685-699 HOEGERMAN SF; RARY JM SPECULATION ON THE ROLE OF TRANSPOSABLE ELEMENTS IN HUMAN GENETIC-DISEASE WITH PARTICULAR ATTENTION TO ACHONDROPLASIA AND THE FRAGILE-X SYNDROME | 10 | 19 |
| 457 | 11 | 29 | 356 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):701-713 FRIEDMAN JM; HOWARDPEEBLES PN INHERITANCE OF FRAGILE-X SYNDROME - AN HYPOTHESIS | 10 | 16 |
| 458 | 18 | 55 | 357 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):723-737 VANDYKE DL; WEISS L MATERNAL EFFECT ON INTELLIGENCE IN FRAGILE-X MALES AND FEMALES | 4 | 8 |
| 459 | 0 | 0 | 358 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 25(1):186-187 DAR H; BAREL H; JAFFE M; WINTER ST THE FRAGILE-X SYNDROME - THE DILEMMA OF SELECTING PATIENTS FOR EXAMINATION | 0 | 1 |
| 460 | 0 | 0 | 359 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 25(1):188-188 SHABTAI F; KLAR D; HART J; HALBRECHT I FRAGILE-X SYNDROME - A GENETIC OR AN INFECTIOUS-DISEASE | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 461 | 8 | 19 | 418 1987 AMERICAN JOURNAL OF MEDICAL GENETICS 26(4):909-914 WENGER SL; HENNESSEY JC; STEELE MW INCREASED SISTER CHROMATID EXCHANGE FREQUENCY AT XQ27-SITE IN AFFECTED FRAGILE-X MALES | 5 | 23 |
| 462 | 5 | 13 | 419 1987 AMERICAN JOURNAL OF MEDICAL GENETICS 26(4):987-990 MULLEY JC; SUTHERLAND GR FRAGILE-X TRANSMISSION AND THE DETERMINATION OF CARRIER PROBABILITIES FOR GENETIC-COUNSELING | 0 | 11 |
| 463 | 12 | 29 | 420 1987 AMERICAN JOURNAL OF MEDICAL GENETICS 27(2):401-417 LOESCH DZ; HAY DA; SUTHERLAND GR; HALLIDAY J; JUDGE C; et al. PHENOTYPIC VARIATION IN MALE-TRANSMITTED FRAGILE-X - GENETIC INFERENCES | 37 | 51 |
| 464 | 7 | 20 | 421 1987 AMERICAN JOURNAL OF MEDICAL GENETICS 27(2):435-448 MULLEY JC; GEDEON AK; THORN KA; BATES LJ; SUTHERLAND GR LINKAGE AND GENETIC-COUNSELING FOR THE FRAGILE-X USING DNA PROBE-52A, PROBE-F9, PROBE-DX13, AND PROBE-ST14 | 17 | 43 |
| 465 | 6 | 10 | 422 1987 AMERICAN JOURNAL OF MEDICAL GENETICS 27(3):731-732 CARPENTER NJ; VEENEMA H; BAKKER E; HOFKER MH; PEARSON PL A NEW DNA PROBE PROXIMAL TO AND CLOSELY LINKED TO FRAGILE-X | 4 | 4 |
| 466 | 7 | 17 | 423 1987 AMERICAN JOURNAL OF MEDICAL GENETICS 28(1):13-15 CHUDLEY AE; DEVONFLINDT R; HAGERMAN RJ COGNITIVE VARIABILITY IN THE FRAGILE X-SYNDROME | 5 | 9 |
| 467 | 1 | 3 | 503 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):1-17 NERI G; OPITZ JM; MIKKELSEN M; JACOBS PA; DAVIES K; et al. CONFERENCE REPORT - 3RD INTERNATIONAL WORKSHOP ON THE FRAGILE-X AND X-LINKED MENTAL-RETARDATION | 6 | 15 |
| 468 | 0 | 0 | 504 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):20-20 KAHKONEN M; ALITALO T; AIRAKSINEN E; MATILAINER R; LAUNIALA K; et al. PREVALENCE OF THE FRAGILE-X OR MARTIN-BELL SYNDROME | 0 | 0 |
| 469 | 0 | 0 | 505 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):20-21 KEREM B; GOITEIN R; SCHAAP T THE DISTRIBUTION OF FRAGILE-X CHROMOSOMES IN AMNIOTIC CELLS CULTURED BY THE INSITU TECHNIQUE | 1 | 1 |
| 470 | 0 | 0 | 506 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):21-21 LEDBETTER DH; LEDBETTER SA HIGH-LEVELS OF FRAGILE-X EXPRESSION IN NORMAL MALES INDUCED BY APHIDICOLIN | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 471 | 0 | 0 | 507 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):22-22 LEISTI J; KAHKONEN M; HERVA R; WINQVIST R; UKKOLA L; et al. THE FRAGILE-X SYNDROME IN NORTHERN FINLAND - A GENEALOGIC STUDY | 0 | 0 |
| 472 | 0 | 0 | 508 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):22-23 OBERLE I; ARVEILER B; WOELFLIN A; HOFKER M; PEARSON P; et al. GENETIC AND PHYSICAL MAPPING OF THE FRAGILE-X REGION - .A. NEW POLYMORPHIC MARKERS .B. IS THE FRAGILE-X SITE A PREFERENTIAL BREAKPOINT IN CHROMOSOME REARRANGEMENTS | 0 | 0 |
| 473 | 0 | 0 | 509 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):23-24 RUDELLI R; MADRID R; BROWN WT FURTHER NEUROPATHOLOGICAL OBSERVATIONS IN ADULT FRAGILE-X | 0 | 0 |
| 474 | 0 | 0 | 510 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):25-25 TOMMERUP N; REINTOFT I; RESKENIELSEN E; BRONDUMNIELSEN K; MIKKELSEN M UNSUSPECTED PRENATAL-DIAGNOSIS OF THE FRAGILE-X | 0 | 1 |
| 475 | 0 | 0 | 511 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):26-26 TOMMERUP N; TRANEBJAERG L; TONNESEN T; KASTERN W; HANSEN H; et al. IDENTICAL EXPRESSION OF THE FRAGILE-X BUT DISCORDANT CLINICAL MANIFESTATIONS IN MONOZYGOTIC TWINS WITH MARTIN-BELL SYNDROME | 0 | 0 |
| 476 | 0 | 0 | 512 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):26-27 TURNER G; PARTINGTON MW; ROBINSON H; LATHAM M; KENNY J; et al. THE PROS AND CONS OF PREVENTIVE SCREENING FOR THE FRAGILE (X) | 0 | 0 |
| 477 | 196 | 429 | 513 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):31-60 SPANO LM; OPITZ JM BIBLIOGRAPHY ON X-LINKED MENTAL-RETARDATION, THE FRAGILE-X AND RELATED SUBJECTS-IV (1988) | 0 | 1 |
| 478 | 0 | 18 | 514 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):77-82 PHELAN MC; STEVENSON RE; COLLINS JL; TRENT HE FRAGILE-X SYNDROME AND NEOPLASIA | 7 | 13 |
| 479 | 8 | 20 | 515 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):83-98 WALDSTEIN G; HAGERMAN R AORTIC HYPOPLASIA AND CARDIAC VALVULAR ABNORMALITIES IN A BOY WITH FRAGILE-X SYNDROME | 5 | 5 |
| 480 | 4 | 16 | 516 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):99-107 FILIPPI G; PECILE V; RINALDI A; SINISCALCO M FRAGILE-X MUTATION AND KLINEFELTER SYNDROME - A REAPPRAISAL | 9 | 13 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 481 | 4 | 9 | 517 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):109-113 FRYNS JP; VANDENBERGHE H THE CONCURRENCE OF KLINEFELTER SYNDROME AND FRAGILE-X SYNDROME | 14 | 17 |
| 482 | 5 | 22 | 518 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):115-121 WATSON MS; BREG WR; PAULS D; BROWN WT; CARROLL AJ; et al. ANEUPLOIDY AND THE FRAGILE-X SYNDROME | 6 | 8 |
| 483 | 16 | 49 | 519 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):123-142 PROUTY LA; ROGERS RC; STEVENSON RE; DEAN JH; PALMER KK; et al. FRAGILE-X SYNDROME - GROWTH, DEVELOPMENT, AND INTELLECTUAL FUNCTION | 28 | 36 |
| 484 | 3 | 9 | 520 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):143-147 NIELSEN KB GROWTH-PATTERN IN BOYS WITH FRAGILE-X | 3 | 3 |
| 485 | 3 | 4 | 521 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):165-168 BUTLER MG; ALLEN GA; SINGH DN; CARPENTER NJ; HALL BD PHOTOANTHROPOMETRIC ANALYSIS OF INDIVIDUALS WITH THE FRAGILE-X SYNDROME | 6 | 10 |
| 486 | 6 | 11 | 522 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):177-183 MILONE G; CONTI L; RIZZO R; SANFILIPPO S; SAMMITO V; et al. A DERMATOGLYPHIC STUDY OF A GROUP OF SICILIAN CHILDREN WITH FRAGILE-X SYNDROME | 1 | 2 |
| 487 | 13 | 27 | 523 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):191-200 KEMPER MB; HAGERMAN RJ; ALTSHULSTARK D COGNITIVE PROFILES OF BOYS WITH THE FRAGILE-X SYNDROME | 58 | 77 |
| 488 | 1 | 3 | 524 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):201-205 BROWN WT; RUDELLI RD; WISNIEWSKI HM FRAGILE-X SYNDROME - NEUROPATHOLOGY CENTER | 1 | 1 |
| 489 | 10 | 36 | 525 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):213-225 WOLFF PH; GARDNER J; LAPPEN J; PACCIA J; MERYASH D VARIABLE EXPRESSION OF THE FRAGILE-X SYNDROME IN HETEROZYGOUS FEMALES OF NORMAL INTELLIGENCE | 28 | 35 |
| 490 | 2 | 4 | 526 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):227-230 HOWARDPEEBLES PN; BROWN WT THE FRAGILE-X SYNDROME - VARIABILITY OF EXPRESSION IN CARRIER FEMALES | 3 | 4 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 491 | 2 | 8 | 527 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):231-236 SUTHERS GK; TURNER G; MULLEY JC CASE-REPORT - FRAGILE-X SYNDROME AND NEPHROGENIC DIABETES-INSIPIDUS | 1 | 2 |
| 492 | 1 | 2 | 528 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):237-238 EINFELD SL AUTISM AND THE FRAGILE-X SYNDROME | 4 | 6 |
| 493 | 11 | 14 | 529 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):337-345 PURVISSMITH SG; LAING S; SUTHERLAND GR; BAKER E PRENATAL-DIAGNOSIS OF THE FRAGILE-X - THE AUSTRALASIAN EXPERIENCE | 0 | 14 |
| 494 | 2 | 8 | 530 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):347-354 SHAPIRO LR; WILMOT PL; MURPHY PD; BREG WR EXPERIENCE WITH MULTIPLE APPROACHES TO THE PRENATAL-DIAGNOSIS OF THE FRAGILE-X SYNDROME - AMNIOTIC-FLUID, CHORIONIC VILLI, FETAL BLOOD AND MOLECULAR METHODS | 12 | 19 |
| 495 | 22 | 61 | 531 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):355-368 MCKINLEY MJ; KEARNEY LU; NICOLAIDES KH; GOSDEN CM; WEBB TP; et al. PRENATAL-DIAGNOSIS OF FRAGILE-X SYNDROME BY PLACENTAL (CHORIONIC VILLI) BIOPSY CULTURE | 8 | 13 |
| 496 | 3 | 4 | 532 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):369-376 SANFILIPPO S; RAGUSA RM; SCILLATO F; RUGGERI M; NERI G FRAGILE-X EXPRESSION IN NORMAL AND MENTALLY-RETARDED SUBJECTS - EFFECT OF TREATMENT WITH AN ANTIFOLIC AGENT | 0 | 4 |
| 497 | 12 | 44 | 533 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):377-392 HAGERMAN RJ; MURPHY MA; WITTENBERGER MD A CONTROLLED TRIAL OF STIMULANT MEDICATION IN CHILDREN WITH THE FRAGILE-X SYNDROME | 25 | 51 |
| 498 | 16 | 23 | 534 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):393-399 FISCH GS; COHEN IL; GROSS AC; JENKINS V; JENKINS EC; et al. FOLIC-ACID TREATMENT OF FRAGILE-X MALES - A FURTHER STUDY | 4 | 9 |
| 499 | 3 | 8 | 535 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):401-406 FRYNS JP; VANDENBERGHE H INACTIVATION PATTERN OF THE FRAGILE-X IN HETEROZYGOUS CARRIERS | 7 | 11 |
| 500 | 3 | 3 | 536 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):417-422 TOMMERUP N; LAING S; CHRISTENSEN IJ; TURNER G SCREENING FOR THE FRAGILE-X - HOW MANY CELLS SHOULD WE ANALYZE | 6 | 8 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 501 | 1 | 2 | 537 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):423-428 TURNER G; PARTINGTON MW FRAGILE(X) EXPRESSION, AGE AND THE DEGREE OF INTELLECTUAL HANDICAP IN THE MALE | 4 | 5 |
| 502 | 21 | 49 | 538 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):435-442 KRAWCZUN MS; JENKINS EC; BROWN WT; SILVERMAN WP FRAGILE-X EXPRESSION IN SHORT-TERM WHOLE-BLOOD CULTURES IS AFFECTED BY CELL-DENSITY | 2 | 3 |
| 503 | 1 | 7 | 539 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):443-450 NOLIN SL; JENKINS EC; BROWN WT; DOBKIN CS INSITU NICK TRANSLATION OF THE FRAGILE-X REGION | 1 | 2 |
| 504 | 1 | 3 | 540 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):455-457 HOWARDPEEBLES P; FROSTERISKENIUS U FRAGILE-X TESTING IN MOTHERS OF TRANSMITTING MALES | 0 | 1 |
| 505 | 2 | 13 | 541 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):459-471 THODE A; LAING S; PARTINGTON MW; TURNER G IS THERE A FRAGILE(X) NEGATIVE MARTIN-BELL SYNDROME | 2 | 6 |
| 506 | 14 | 27 | 542 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):531-542 SCHWARTZ CE; PHELAN MC; BRIGHTHARP C; PANCOAST I; HOWARDPEEBLES PN; et al. FRAGILE-X SYNDROME - LINKAGE ANALYSIS IN BLACK AND WHITE-POPULATIONS | 4 | 4 |
| 507 | 8 | 22 | 543 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):543-550 HEILIG R; OBERLE I; ARVEILER B; HANAUER A; VIDAUD M; et al. IMPROVED DNA MARKERS FOR EFFICIENT ANALYSIS OF FRAGILE-X FAMILIES | 11 | 33 |
| 508 | 12 | 22 | 544 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):551-566 BROWN WT; YE W; GROSS AC; CHAN CB; DOBKIN CS; et al. MULTIPOINT LINKAGE OF 9 ANONYMOUS PROBES TO HPRT, FACTOR-IX, AND FRAGILE-X | 8 | 25 |
| 509 | 5 | 13 | 545 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):567-580 MULLEY J; TURNER G; BAIN S; SUTHERLAND GR LINKAGE BETWEEN THE FRAGILE-X AND F9, DXS52 (ST14), DXS98 (4D-8) AND DXS105 (CX55.7) | 13 | 20 |
| 510 | 4 | 18 | 546 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):613-623 WARREN ST; ZHANG F; SUTCLIFFE JS; PETERS JF STRATEGY FOR MOLECULAR-CLONING OF THE FRAGILE-X SITE DNA | 7 | 12 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 511 | 3 | 4 | 547 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):625-631 SHERMAN SL; TURNER G; SHEFFIELD L; LAING S; ROBINSON H INVESTIGATION OF THE TWINNING RATE IN FAMILIES WITH THE FRAGILE-X SYNDROME | 6 | 8 |
| 512 | 4 | 5 | 548 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):633-639 SHERMAN SL; TURNER G; ROBINSON H; LAING S INVESTIGATION OF THE SEGREGATION OF THE FRAGILE-X MUTATION IN DAUGHTERS OF OBLIGATE CARRIER WOMEN | 5 | 7 |
| 513 | 7 | 16 | 549 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):641-654 SCHWARTZ CE; PHELAN MC; PULLIAM LH; WILKES G; VANNER LV; et al. FRAGILE-X SYNDROME - INCIDENCE, CLINICAL AND CYTOGENETIC FINDINGS IN THE BLACK AND WHITE-POPULATIONS OF SOUTH-CAROLINA | 12 | 15 |
| 514 | 32 | 50 | 550 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):655-663 FISCH GS; COHEN IL; JENKINS EC; BROWN WT SCREENING DEVELOPMENTALLY DISABLED MALE POPULATIONS FOR FRAGILE-X - THE EFFECT OF SAMPLE-SIZE | 18 | 22 |
| 515 | 6 | 10 | 551 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):665-672 NERI G; SANFILIPPO S; PAVONE L; MOLLICA F; BARBERI I; et al. THE FRAGILE-X IN SICILY - AN EPIDEMIOLOGICAL SURVEY | 10 | 16 |
| 516 | 8 | 12 | 552 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):673-679 HOLMGREN G; BLOMQUIST HK; DRUGGE U; GUSTAVSON KH FRAGILE-X FAMILIES IN A NORTHERN SWEDISH COUNTY - A GENEALOGICAL STUDY DEMONSTRATING APPARENT PATERNAL TRANSMISSION FROM THE 18TH-CENTURY | 10 | 10 |
| 517 | 7 | 21 | 553 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):681-688 WARREN ST FRAGILE-X SYNDROME - A HYPOTHESIS REGARDING THE MOLECULAR MECHANISM OF THE PHENOTYPE | 5 | 6 |
| 518 | 2 | 5 | 554 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):693-696 LAIRD CD FRAGILE-X MUTATION PROPOSED TO BLOCK COMPLETE REACTIVATION IN FEMALES OF AN INACTIVE X-CHROMOSOME | 7 | 10 |
| 519 | 8 | 28 | 555 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):697-702 SHABTAI F; HART J; KLAR D; BICHACHO S; HALBRECHT I FRAGILE-X EXPRESSION IN MARTIN-BELL SYNDROME, INTELLECTUALLY NORMAL INDIVIDUALS, AND NEOPLASIA, INTERPRETED BY A VIRAL HYPOTHESIS | 2 | 3 |
| 520 | 2 | 17 | 556 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 31(2):407-414 REISS AL; PATEL S; KUMAR AJ; FREUND L PRELIMINARY COMMUNICATION - NEUROANATOMICAL VARIATIONS OF THE POSTERIOR-FOSSA IN MEN WITH THE FRAGILE-X (MARTIN-BELL) SYNDROME | 16 | 38 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 521 | 3 | 4 | 557 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 31(4):733-734 WILSON DP; CARPENTER NJ; BERKOVITZ G THYROID-FUNCTION IN MEN WITH FRAGILE X-LINKED MR | 3 | 3 |
| 522 | 8 | 13 | 558 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 31(4):735-739 MAVROU A; SYRROU M; TSENGHI C; AGELAKIS M; YOUROUKOS S; et al. MARTIN-BELL SYNDROME IN GREECE, WITH REPORT OF ANOTHER 47,XXY FRAGILE X PATIENT | 7 | 10 |
| 523 | 5 | 12 | 559 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 31(4):753-765 SHERMAN SL; ROGATKO A; TURNER G RECURRENCE RISKS FOR RELATIVES IN FAMILIES WITH AN ISOLATED CASE OF THE FRAGILE X SYNDROME | 11 | 15 |
| 524 | 2 | 15 | 560 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 31(4):767-773 BUTLER MG; FLETCHER M; GALE DD; MEANEY FJ; MCLEOD DR; et al. METACARPOPHALANGEAL PATTERN PROFILE ANALYSIS IN FRAGILE-X SYNDROME | 4 | 8 |
| 525 | 5 | 12 | 561 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 31(4):775-778 BUTLER MG; DEV VG; SHAH D; ULM JE; WILMOT PL; et al. THE USE OF EARLY SIMULTANEOUS PERCUTANEOUS UMBILICAL BLOOD-SAMPLING (PUBS) AND AMNIOCENTESIS FOR PRENATAL FRAGILE-X CHROMOSOME DIAGNOSIS | 0 | 0 |
| 526 | 2 | 10 | 562 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 31(4):779-781 BUTLER MG; NAJJAR JL DO SOME PATIENTS WITH FRAGILE-X SYNDROME HAVE PRECOCIOUS PUBERTY | 13 | 15 |
| 527 | 7 | 18 | 620 1989 AMERICAN JOURNAL OF MEDICAL GENETICS 33(1):92-99 BRIDGE PJ; LILLICRAP DP MOLECULAR DIAGNOSIS OF THE FRAGILE-X [FRA-(X)] SYNDROME - CALCULATION OF RISKS BASED ON FLANKING DNA MARKERS IN SMALL PHASE-UNKNOWN FAMILIES | 0 | 4 |
| 528 | 5 | 19 | 621 1989 AMERICAN JOURNAL OF MEDICAL GENETICS 33(2):200-208 LOESCH DZ; WILSON SR MULTIVARIATE-ANALYSIS OF BODY SHAPE IN FRAGILE-X (MARTIN-BELL) SYNDROME | 2 | 5 |
| 529 | 11 | 30 | 622 1989 AMERICAN JOURNAL OF MEDICAL GENETICS 33(4):513-518 HAGERMAN RJ; SCHREINER RA; KEMPER MB; WITTENBERGER MD; ZAHN B; et al. LONGITUDINAL IQ CHANGES IN FRAGILE-X MALES | 37 | 49 |
| 530 | 21 | 44 | 623 1989 AMERICAN JOURNAL OF MEDICAL GENETICS 34(2):187-193 EINFELD S; MOLONY H; HALL W AUTISM IS NOT ASSOCIATED WITH THE FRAGILE-X SYNDROME | 31 | 53 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 531 | 10 | 14 | 624 1989 AMERICAN JOURNAL OF MEDICAL GENETICS 34(2):302-303 COHEN IL; BROWN WT; JENKINS EC; KRAWCZUN MS; FRENCH JH; et al. FRAGILE-X SYNDROME IN FEMALES WITH AUTISM | 13 | 16 |
| 532 | 19 | 43 | 683 1990 AMERICAN JOURNAL OF MEDICAL GENETICS 35(1):22-27 MINGRONINETTO RC; ROSENBERG C; VIANNAMORGANTE AM; PAVANELLO RDM FRAGILE-X FREQUENCY IN A MENTALLY-RETARDED POPULATION IN BRAZIL | 5 | 8 |
| 533 | 7 | 30 | 684 1990 AMERICAN JOURNAL OF MEDICAL GENETICS 35(1):28-35 GRIGSBY JP; KEMPER MB; HAGERMAN RJ; MYERS CS NEUROPSYCHOLOGICAL DYSFUNCTION AMONG AFFECTED HETEROZYGOUS FRAGILE-X FEMALES | 24 | 29 |
| 534 | 9 | 16 | 685 1990 AMERICAN JOURNAL OF MEDICAL GENETICS 36(1):122-125 VANROY BC; WILLEMS PJ; VITS LJ; CEULEMANS BP; COUCKE PJ; et al. 2 BROTHERS WITH MENTAL-RETARDATION DISCORDANT FOR THE FRAGILE-X SYNDROME | 4 | 4 |
| 535 | 6 | 17 | 686 1990 AMERICAN JOURNAL OF MEDICAL GENETICS 37(2):265-267 MOORE PSJ; CHUDLEY AE; WINTER JSD TRUE PRECOCIOUS PUBERTY IN A GIRL WITH THE FRAGILE X-SYNDROME | 10 | 13 |
| 536 | 1 | 2 | 687 1990 AMERICAN JOURNAL OF MEDICAL GENETICS 37(3):433-433 MEISNER LF FRAGILE-X FREQUENCY | 0 | 0 |
| 537 | 1 | 1 | 688 1990 AMERICAN JOURNAL OF MEDICAL GENETICS 37(3):434-434 MINGRONINETTO RC; ROSENBERG C; VIANNAMORGANTE AM; PAVANELLO RCM FRAGILE-X FREQUENCY - RESPONSE | 0 | 0 |
| 538 | 12 | 39 | 787 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):158-172 BROWN WT; JENKINS E; NERI G; LUBS H; SHAPIRO LR; et al. 4TH INTERNATIONAL WORKSHOP ON THE FRAGILE-X AND X-LINKED MENTAL-RETARDATION | 1 | 7 |
| 539 | 0 | 0 | 788 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):173-185 SPANO LM; OPITZ JM BIBLIOGRAPHY ON X-LINKED MENTAL-RETARDATION, THE FRAGILE-X, AND RELATED SUBJECTS .5. (1991) | 0 | 1 |
| 540 | 12 | 19 | 789 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):251-255 NOLIN SL; SNIDER DA; JENKINS EC; BROWN WT; KRAWCZUN M; et al. FRAGILE-X SCREENING-PROGRAM IN NEW-YORK-STATE | 18 | 24 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 541 | 1 | 1 | 790 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):256-259 LAING S; PARTINGTON M; ROBINSON H; TURNER G CLINICAL SCREENING SCORE FOR THE FRAGILE-X (MARTIN-BELL) SYNDROME | 25 | 29 |
| 542 | 7 | 32 | 791 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):260-268 BUTLER MG; ALLEN GA; HAYNES JL; SINGH DN; WATSON MS; et al. ANTHROPOMETRIC COMPARISON OF MENTALLY-RETARDED MALES WITH AND WITHOUT THE FRAGILE-X SYNDROME | 16 | 22 |
| 543 | 11 | 14 | 792 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):269-274 CRONISTER A; SCHREINER R; WITTENBERGER M; AMIRI K; HARRIS K; et al. HETEROZYGOUS FRAGILE-X FEMALE - HISTORICAL, PHYSICAL, COGNITIVE, AND CYTOGENETIC FEATURES | 39 | 57 |
| 544 | 12 | 21 | 793 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):283-287 HAGERMAN RJ; AMIRI K; CRONISTER A FRAGILE-X CHECKLIST | 47 | 64 |
| 545 | 1 | 8 | 794 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):288-289 ZHAO Y; SHEN Y; LIU Y; ZHANG JC; YE LZ; et al. FRAGILE-X SYNDROME (MARTIN-BELL SYNDROME) IN CHINA | 1 | 1 |
| 546 | 12 | 23 | 795 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):292-297 BROWN WT; GROSS A; GOONEWARDENA P; FERRANDO C; DOBKIN C; et al. DETECTION OF FRAGILE-X NON-PENETRANT MALES BY DNA MARKER ANALYSIS | 4 | 4 |
| 547 | 16 | 47 | 796 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):298-304 GLASS IA; PIRRIT LA; WHITE EM; BELL MV; DAVIES KE; et al. LINKAGE ANALYSIS IN THE FRAGILE-X SYNDROME USING MULTIPLE DISTAL XQ POLYMORPHIC DNA MARKERS | 2 | 2 |
| 548 | 2 | 9 | 797 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):305-310 MURPHY PD; WATSON MS; SHAPIRO LR; WILMOT PL; BREG WR DNA-BASED GENETIC TESTING IN 50 FRAGILE-X FAMILIES | 2 | 2 |
| 549 | 7 | 20 | 798 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):311-318 CARPENTER NJ DNA LINKAGE ANALYSIS OF 26 FAMILIES WITH FRAGILE-X SYNDROME | 1 | 1 |
| 550 | 9 | 14 | 799 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):319-321 DAHL N; MALMGREN H; PETTERSSON U; HOLMGREN G; SEEMANOVA E; et al. CARRIER DETECTION OF THE FRAGILE-X SYNDROME USING FLANKING LOCI DXS98, DXS105, AND DXS304 | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 551 | 14 | 31 | 800 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):322-327 GOONEWARDENA P; BROWN WT; GROSS AC; FERRANDO C; DOBKIN C; et al. LINKAGE ANALYSIS OF THE FRAGILE-X SYNDROME USING A NEW DNA MARKER U6.2 DEFINING LOCUS DXS304 | 1 | 1 |
| 552 | 6 | 18 | 801 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):328-331 VANOOST BA; SMITS A; DREESEN JCFM; SMEETS D; PERDON L; et al. MULTIPOINT LINKAGE ANALYSIS OF DXS369 AND DXS304 IN FRAGILE-X FAMILIES | 4 | 7 |
| 553 | 3 | 20 | 802 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):343-346 BROWN WT; GROSS AC; GOONEWARDENA P; FERRANDO C; DOBKIN C; et al. LINKAGE IN FRAGILE-X FAMILIES OF 3 DISTAL FLANKING MARKERS - ST14, DX13, AND F8 | 1 | 2 |
| 554 | 4 | 4 | 803 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):347-348 ROMANO V; MASCALI G; CHIAVETTA V; RAGUSA RM; BARLETTA C; et al. RFLP ANALYSIS IN 5 SICILIAN FAMILIES WITH THE FRAGILE-X SYNDROME | 0 | 0 |
| 555 | 16 | 20 | 804 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):349-353 CARPENTER NJ; THIBODEAU SN; BROWN WT LINKAGE RELATIONSHIPS BETWEEN DXS105, DXS98, AND OTHER POLYMORPHIC DNA MARKERS FLANKING THE FRAGILE-X LOCUS | 2 | 3 |
| 556 | 7 | 11 | 805 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):363-366 DRUGGE U; BLOMQUIST HK; GUSTAVSON KH; HOLMGREN G FRAGILE-X FAMILIES IN A NORTHERN SWEDISH COUNTY - A GENEALOGICAL STUDY OF POSSIBLY AFFECTED INDIVIDUALS IN THE 19TH-CENTURY | 2 | 2 |
| 557 | 12 | 18 | 806 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):367-369 PELLISSIER MC; VOELCKEL MA; PIQUET C; MATTEI MG; MATTEI JF TRANSMISSION OF MENTAL-RETARDATION WITH FRAGILE-X SITE BY 2 NORMAL TRANSMITTER BROTHERS | 0 | 0 |
| 558 | 13 | 23 | 807 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):370-373 BROOKS SS; COHEN I; FERRANDO C; JENKINS EC; BROWN WT; et al. CYTOGENETICALLY NEGATIVE, LINKAGE POSITIVE FRAGILE-X SYNDROME | 0 | 1 |
| 559 | 13 | 25 | 808 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):374-377 VOELCKEL MA; PELLISSIER MC; PIQUET C; NGUYEN C; BOCCACCIO I; et al. FRAGILE-X SYNDROME IN AN EXTENDED FAMILY WITH SPECIAL REFERENCE TO AN AFFECTED MALE WITH KLINEFELTER SYNDROME | 2 | 2 |
| 560 | 1 | 5 | 809 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):378-379 DOBKIN CS; DRISCOLL MC; FERRANDO C POLYMERASE CHAIN-REACTION DETECTION OF THE DDE-I POLYMORPHISM IN THE FACTOR-IX GENE FOR FRAGILE-X LINKAGE ANALYSIS | 0 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 561 | 4 | 15 | 810 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):380-383 PERGOLIZZI R; BROWN WT; GOONEWARDENA P; BHAN R; DOBKIN C; et al. MOLECULAR CHARACTERIZATION OF A DNA PROBE, U6.2, LOCATED CLOSE TO THE FRAGILE-X LOCUS | 0 | 0 |
| 562 | 11 | 25 | 811 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):391-395 LAIRD CD POSSIBLE ERASURE OF THE IMPRINT ON A FRAGILE-X CHROMOSOME WHEN TRANSMITTED BY A MALE | 8 | 15 |
| 563 | 4 | 7 | 812 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):396-399 SHERMAN SL COLLABORATIVE PROSPECTIVE-STUDY OF THE FRAGILE-X SYNDROME - REQUEST FOR PARTICIPATION | 2 | 2 |
| 564 | 4 | 23 | 813 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):400-403 JACKY PB; AHUJA YR; ANYANEYEBOA K; BREG WR; CARPENTER NJ; et al. GUIDELINES FOR THE PREPARATION AND ANALYSIS OF THE FRAGILE-X CHROMOSOME IN LYMPHOCYTES | 31 | 44 |
| 565 | 7 | 16 | 814 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):404-407 FISCH GS; SILVERMAN W; JENKINS EC GENETIC AND OTHER FACTORS THAT CONTRIBUTE TO VARIABILITY IN CYTOGENETIC EXPRESSION IN FRAGILE-X MALES | 4 | 7 |
| 566 | 0 | 4 | 815 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):408-410 SHAPIRO LR; WILMOT PL; SHAPIRO DA; PETTERSEN IM; CASAMASSIMA AC CYTOGENETIC DIAGNOSIS OF THE FRAGILE-X SYNDROME - EFFICIENCY, UTILIZATION, AND TRENDS | 3 | 3 |
| 567 | 1 | 7 | 816 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):416-417 JENKINS LS; GRUENERT DC; JENKINS EC; SCHONBERG SA TRANSFORMATION AND ESTABLISHMENT OF FRAGILE-X CELL-LINES FROM AMNIOCYTES | 1 | 1 |
| 568 | 4 | 16 | 817 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):418-420 LEDBETTER SA; SCHWARTZ CE; DAVIES KE; LEDBETTER DH NEW SOMATIC-CELL HYBRIDS FOR PHYSICAL MAPPING IN DISTAL XQ AND THE FRAGILE-X REGION | 0 | 14 |
| 569 | 12 | 22 | 818 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):421-424 ROSENBERG C; VIANNAMORGANTE AM; OTTO PA; NAVAJAS L EFFECT OF X-INACTIVATION ON FRAGILE-X FREQUENCY AND MENTAL-RETARDATION | 4 | 5 |
| 570 | 6 | 20 | 819 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):429-433 KIMCHISARFATY C; GOITEIN R; KEREM B; WERNER M; MEIDAN B; et al. ENDOREDUPLICATION AND POLYPLOIDY IN FRAGILE-X CELLS INDUCED BY METHOTREXATE AND FLUORODEOXYURIDINE - IMPLICATIONS FOR DIAGNOSIS | 1 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 571 | 10 | 28 | 820 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):440-444 KUPKE KG; SORENG AL; MULLER U ORIGIN OF THE SUPERNUMERARY X-CHROMOSOME IN A PATIENT WITH FRAGILE-X AND KLINEFELTER SYNDROME | 7 | 9 |
| 572 | 2 | 4 | 821 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):445-446 HOWARDPEEBLES PN FRAGILE-X EXPRESSION - USE OF A DOUBLE INDUCTION SYSTEM | 2 | 4 |
| 573 | 4 | 11 | 822 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):453-455 SHAPIRO LR; WILMOT PL; MURPHY PD PRENATAL-DIAGNOSIS OF THE FRAGILE-X SYNDROME - POSSIBLE END OF THE EXPERIMENTAL PHASE FOR AMNIOTIC-FLUID | 5 | 6 |
| 574 | 2 | 33 | 823 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):456-463 KRAWCZUN MS; JENKINS EC; DUNCAN CJ; STARKHOUCK SL; KUNAPORN S; et al. DISTRIBUTION OF AUTOSOMAL FRAGILE SITES IN SPECIMENS CULTURED FOR PRENATAL FRAGILE-X DIAGNOSIS | 1 | 1 |
| 575 | 1 | 8 | 824 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):464-466 JENKINS EC; BROOKS SE; STARKHOUCK SL; DUNCAN CJ; BROOKS SLS; et al. SV40-TRANSFORMED FRAGILE(X) AMNIOCYTES | 1 | 1 |
| 576 | 9 | 34 | 825 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):481-487 FISCH GS; ARINAMI T; FROSTERISKENIUS U; FRYNS JP; CURFS LM; et al. RELATIONSHIP BETWEEN AGE AND IQ AMONG FRAGILE-X MALES - A MULTICENTER STUDY | 13 | 14 |
| 577 | 6 | 20 | 826 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):488-492 DEVONFLINDT R; BYBEL B; CHUDLEY AE; LOPES F SHORT-TERM-MEMORY AND COGNITIVE VARIABILITY IN ADULT FRAGILE-X FEMALES | 7 | 9 |
| 578 | 3 | 21 | 827 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):493-497 SUDHALTER V; SCARBOROUGH HS; COHEN IL SYNTACTIC DELAY AND PRAGMATIC DEVIANCE IN THE LANGUAGE OF FRAGILE-X MALES | 23 | 31 |
| 579 | 3 | 19 | 828 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):498-502 COHEN IL; VIETZE PM; SUDHALTER V; JENKINS EC; BROWN WT EFFECTS OF AGE AND COMMUNICATION LEVEL ON EYE CONTACT IN FRAGILE-X MALES AND NON-FRAGILE-X AUTISTIC MALES | 22 | 33 |
| 580 | 7 | 15 | 829 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):503-504 CRONISTER A; HAGERMAN RJ; WITTENBERGER M; AMIRI K MENTAL IMPAIRMENT IN CYTOGENETICALLY POSITIVE FRAGILE-X FEMALES | 14 | 15 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 581 | 7 | 12 | 830 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):505-508 BRAINARD SS; SCHREINER RA; HAGERMAN RJ COGNITIVE PROFILES OF THE CARRIER FRAGILE-X WOMAN | 21 | 25 |
| 582 | 3 | 9 | 831 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):509-509 HECHT F SEIZURE DISORDERS IN THE FRAGILE-X CHROMOSOME SYNDROME | 3 | 7 |
| 583 | 3 | 10 | 832 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):511-513 MUSUMECI SA; FERRI R; ELIA M; COLOGNOLA RM; BERGONZI P; et al. EPILEPSY AND FRAGILE-X SYNDROME - A FOLLOW-UP-STUDY | 21 | 36 |
| 584 | 5 | 15 | 833 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 39(3):374-375 MOORE PSJ; CHUDLEY AE; WINTER JSD PITUITARY-GONADAL AXIS IN PREPUBERTAL BOYS WITH THE FRAGILE-X SYNDROME | 5 | 7 |
| 585 | 14 | 31 | 834 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 40(2):234-243 CIANCHETTI C; SANNIOFANCELLO G; FRATTA AL; MANCONI F; ORANO A; et al. NEUROPSYCHOLOGICAL, PSYCHIATRIC, AND PHYSICAL MANIFESTATIONS IN 149 MEMBERS FROM 18 FRAGILE-X FAMILIES | 16 | 19 |
| 586 | 2 | 4 | 835 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 40(4):523-523 DREESEN JCFM; SMITS A; BRUNNER H RISK CALCULATIONS IN THE FRAGILE-X SYNDROME | 0 | 0 |
| 587 | 2 | 5 | 836 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 40(4):524-524 WILLEMS PJ; VANROY B; RAEYMAEKERS P; OOSTRA B RISK CALCULATIONS IN THE FRAGILE-X SYNDROME - REPLY | 0 | 0 |
| 588 | 2 | 12 | 837 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 41(3):275-278 LACHIEWICZ AM; HOEGERMAN SF; HOLMGREN G; HOLMBERG E; ARINBJARNARSON K ASSOCIATION OF THE ROBIN SEQUENCE WITH THE FRAGILE-X SYNDROME | 5 | 8 |
| 589 | 10 | 39 | 838 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 41(3):289-294 HINTON VJ; BROWN WT; WISNIEWSKI K; RUDELLI RD ANALYSIS OF NEOCORTEX IN 3 MALES WITH THE FRAGILE-X SYNDROME | 92 | 134 |
| 590 | 8 | 14 | 912 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 42(2):184-186 FINUCANE BM; JAEGER E; DUNN E; SCOTT CI STUDY OF COLOR-VISION IN FRAGILE-X SYNDROME | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 591 | 8 | 19 | 913 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 42(6):835-838 RAMOS FJ; EMANUEL BS; SPINNER NB FREQUENCY OF THE COMMON FRAGILE SITE AT XQ27.2 UNDER CONDITIONS OF THYMIDYLATE STRESS - IMPLICATIONS FOR CYTOGENETIC DIAGNOSIS OF THE FRAGILE-X SYNDROME | 0 | 1 |
| 592 | 24 | 31 | 914 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):5-27 MANDEL JL; HAGERMAN R; FROSTER U; BROWN WT; JENKINS EC; et al. 5TH INTERNATIONAL WORKSHOP ON THE FRAGILE-X AND X-LINKED MENTAL-RETARDATION | 5 | 8 |
| 593 | 9 | 27 | 915 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):28-34 FISCH GS; SHAPIRO LR; SIMENSEN R; SCHWARTZ CE; FRYNS JP; et al. LONGITUDINAL CHANGES IN IQ AMONG FRAGILE-X MALES - CLINICAL-EVIDENCE OF MORE THAN ONE MUTATION | 12 | 12 |
| 594 | 12 | 22 | 916 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):35-46 REISS AL; FREUND L BEHAVIORAL-PHENOTYPE OF FRAGILE-X SYNDROME - DSM-III-R AUTISTIC BEHAVIOR IN MALE-CHILDREN | 55 | 74 |
| 595 | 30 | 56 | 917 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):47-55 FISCH GS IS AUTISM ASSOCIATED WITH THE FRAGILE-X SYNDROME | 20 | 36 |
| 596 | 10 | 18 | 918 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):56-60 EINFELD S; HALL W BEHAVIOR PHENOTYPE OF THE FRAGILE X SYNDROME | 6 | 12 |
| 597 | 2 | 9 | 919 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):61-64 REISS AL; CIANCHETTI C; COHEN IL; DEVRIES B; HAGERMAN R; et al. BRIEF SCREENING QUESTIONNAIRE FOR DETERMINING AFFECTED STATE IN FRAGILE-X SYNDROME - A CONSENSUS RECOMMENDATION | 2 | 3 |
| 598 | 4 | 12 | 920 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):65-71 SUDHALTER V; MARANION M; BROOKS P EXPRESSIVE SEMANTIC DEFICIT IN THE PRODUCTIVE LANGUAGE OF MALES WITH FRAGILE-X SYNDROME | 19 | 21 |
| 599 | 11 | 18 | 921 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):72-77 LACHIEWICZ AM ABNORMAL BEHAVIORS OF YOUNG GIRLS WITH FRAGILE-X SYNDROME | 20 | 27 |
| 600 | 1 | 14 | 922 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):78-86 MAZZOCCO MMM; HAGERMAN RJ; PENNINGTON BF PROBLEM-SOLVING LIMITATIONS AMONG CYTOGENETICALLY EXPRESSING FRAGILE-X WOMEN | 24 | 32 |