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Nodes: 2369
Authors: 4634,
Journals: 373,
Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by NCR.
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| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 2201 | 0 | 0 | 1803 1999 JOURNAL OF MEDICAL GENETICS 36:S64-S64 Lazarau L; Warburton SA; Roberts CE; Hughes HE; Bartlett S; Meredith AL; Ravine D Fragile X syndrome carrier females with full mutations inherited from a normal transmitting male | 0 | 0 |
| 2202 | 0 | 0 | 1804 1999 JOURNAL OF MEDICAL GENETICS 36:S65-S65 Chotai K; Payne SJ A fragile-X male mosaic for normal, premutation and full mutation FMR-1 alleles | 0 | 0 |
| 2203 | 0 | 0 | 1807 1999 JOURNAL OF MEDICAL GENETICS 36(2):171-172 De Vries BBA; Halley DJJ; Oostra BA; Niermeijer MF Fragile X syndrome: of POF and premutations | 0 | 0 |
| 2204 | 0 | 0 | 1817 1999 MOLECULAR PSYCHIATRY 4:S56-S56 Fisch GS; Carpenter N; Holden JA; Pandya A; Howard-Peebles PN; Tarleton J Psychopathology in genetic disorders producing cognitive deficits: Adaptive and maladative behavior in the fragile X syndrome, Williams syndrome and neurofibromatosis type 1. | 0 | 0 |
| 2205 | 0 | 0 | 1831 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):18-18 Jin P; Feng Y; Brown V; Warren ST Identification of polyribosomes-associated mRNAs regulated by fragile X mental retardation protein (FMRP) using oligonucleotide microarrays. | 1 | 2 |
| 2206 | 0 | 0 | 1832 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):18-18 Brown V; Ceman S; Jin P; Jin C; Wilkinson KD; Warren ST Messenger RNAs associated with the fragile X mental retardation protein in mouse brain. | 1 | 1 |
| 2207 | 0 | 0 | 1833 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 |
| 2208 | 0 | 0 | 1834 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):26-26 Hagerman RJ; Tassone F; Leehey M; Hills J; Wilson R; Landau W; Grigsby J; Gage B; Hagerman PJ Cerebellar tremor and cerebellar cortical atrophy in older males with the fragile X premutation. | 0 | 0 |
| 2209 | 0 | 0 | 1835 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 |
| 2210 | 0 | 0 | 1836 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2211 | 0 | 0 | 1837 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 |
| 2212 | 0 | 0 | 1838 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 |
| 2213 | 0 | 0 | 1839 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):135-135 Harris SW; Brown KE; Hills JL; Tassone F; Hagerman PJ; Taylor AK; Hagerman RJ Adaptive functioning and molecular relationships in individuals with fragile X syndrome. | 0 | 0 |
| 2214 | 0 | 0 | 1840 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 |
| 2215 | 0 | 0 | 1841 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 |
| 2216 | 0 | 0 | 1842 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 |
| 2217 | 0 | 0 | 1843 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 |
| 2218 | 0 | 0 | 1844 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 |
| 2219 | 0 | 0 | 1845 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):348-348 Dyack S; Steele L; Koultchitski G; Yang Y; Weksberg R; Ray PN; Pearson CE AGG interruptions in the CGG trinucleotide repeat tract of the FMR1 gene may contribute to stability of Fragile X premutations. | 0 | 0 |
| 2220 | 0 | 0 | 1846 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):360-360 Ramos FJ; Mila M; Ortilles M; Rife M; Tazon B; De Diego Y; Willemsen R Validity of the analysis of the FMRP expression in bloodsmears as a screening method for the Fragile X Syndrome. | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2221 | 0 | 0 | 1847 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 |
| 2222 | 0 | 0 | 1848 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 |
| 2223 | 0 | 0 | 1849 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):415-415 Najmabadi H; Taghizadeh F; Teimourian SH; Karimi-Nejad R; Shafeghati Y; Mohammady GB; Al-Madany SN; Hoseiny SS; Karimi-Nejad MH Molecular analysis of Fragile X syndrome in Iranian population. | 0 | 0 |
| 2224 | 0 | 0 | 1850 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):428-428 Brown WT; Ding X; Idrissi AE; Scalia J; Glicksman A; Bauchwitz R; Dobkin C Fragile X transgene and embryonic lethality in mice. | 0 | 0 |
| 2225 | 0 | 0 | 1879 2000 CLINICAL CHEMISTRY 46(6):A206-A206 Boday A; Prusa R; Matoska V Radioactive PCR for the screening and diagnostics of fragile X chromosome syndrome - FRAXA. | 0 | 0 |
| 2226 | 0 | 0 | 1885 2000 EUROPEAN JOURNAL OF NEUROSCIENCE 12:305-305 Beckel-Mitchener AC; Weiler IJ; Klintsova AY; Harms L; Belt B; Spangler CC; Greenough WT Analysis of protein synthesis in Fragile X knockout mice | 0 | 0 |
| 2227 | 0 | 0 | 1887 2000 GENETIC COUNSELING 11(3):281-311 [Anon] ACTS: Of the 9th International Workshop on Fragile X Syndrome and X Linked Mental Retardation August 23-25, 1999, Le Bischenberg, Strasbourg, France - Abstracts | 0 | 0 |
| 2228 | 0 | 0 | 1898 2000 HUMAN REPRODUCTION 15:12-12 Apessos A; Harper J; Delhanty JDA Preimplantation genetic diagnosis of the fragile X syndrome by use of linked polymorphic markers | 0 | 0 |
| 2229 | 0 | 0 | 1899 2000 HUMAN REPRODUCTION 15:47-48 Hundscheid RDL; Sistermans EA; Thomas CMG; Straatman H; Kiemeney LALM; Oostra BA; Smits APT; Braat DDM Shorter reproductive life and a high risk for premature ovarian failure (POF) in women who have inherited fragile X premutations from their fathers | 0 | 0 |
| 2230 | 0 | 0 | 1903 2000 INFANT MENTAL HEALTH JOURNAL 21(4-5):330-330 Ghuman JK; Tierney E; Kau A; Reider E Social interaction problems in infants and preschool children with fragile-X syndrome, Smith-Lemli-Opitz syndrome and other developmental disorders | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2231 | 0 | 0 | 1907 2000 JOURNAL OF COGNITIVE NEUROSCIENCE :57-57 Merin NM; Menon V; White CD; Glover GH; Reiss AL Gaze processing deficits in fragile X syndrome investigated using fMRI | 0 | 0 |
| 2232 | 0 | 0 | 1908 2000 JOURNAL OF COGNITIVE NEUROSCIENCE :98-98 White CD; Menon V; Eliez S; Reiss AL An fMRI study of brain activation in Fragile X Syndrome during a go-nogo task | 0 | 0 |
| 2233 | 0 | 0 | 1909 2000 JOURNAL OF COGNITIVE NEUROSCIENCE :146-146 Kwon H; Menon V; Eliez S; Dyer-Friedman J; Glover GH; Reiss AL Functional neuroanatomy of visuospatial working memory in fragile X syndrome: Relation to behavior and FMR-1 protein expression | 0 | 0 |
| 2234 | 0 | 0 | 1913 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:189-189 Abbeduto L; Kesin E; Pavetto M; Weissman M; O'Brien A; Karadottir S; Cawthon S Theory of mind deficits in mental retardation: a comparison of Down syndrome and fragile-X syndrome | 0 | 0 |
| 2235 | 0 | 0 | 1914 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:222-222 Brown WT; Nolin S; Houck G; Ding X; Glicksman A; Li SY; Rabe A; Dumas R; Haubenstock H; Wen Y; Dobkin C; Jenkins E Progress fragile-X syndrome analysis | 0 | 0 |
| 2236 | 0 | 0 | 1915 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:247-247 Cornish KM; Munir F Profile of memory and attention problems in adults with fragile-X syndrome: Clinical and educational implications | 0 | 0 |
| 2237 | 0 | 0 | 1916 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:273-273 Einfeld SL; Tonge B; Turner G; Parmenter T; Smith A Longitudinal course of behavioural and emotional problems of young persons with Prader-Willi, fragile-X, Williams and Down syndromes | 0 | 0 |
| 2238 | 0 | 0 | 1917 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:305-305 Hagerman RJ; Miller LJ; McGrath-Clarke J; Riley K; Goldson E; Harris SW; Simon J; Church K; Bonnell J; Ognibene TC; McIntosh DN Influence of stimulants on electrodermal studies in fragile-X syndrome | 0 | 0 |
| 2239 | 0 | 0 | 1918 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:317-317 Karrer JH; Hagerman RJ; Karrer RS; Fitzpatrick D; Vavold J; Gora K; Chaney L Genotypic-specific event-related brain potentials among infants and toddlers with fragile-X syndrome and Down syndrome | 1 | 1 |
| 2240 | 0 | 0 | 1919 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:318-318 Hills JL; Wilson R; Sobesky W; Harris SW; Grigsby J; Butler E; Loesch D; Hagerman RJ Executive functioning deficits in adult males with the fragile-X premutation: an emerging phenotype | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2241 | 0 | 0 | 1920 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:374-374 Lung FW; Shu BC Fragile-X syndrome in adolescent prostitutes | 0 | 0 |
| 2242 | 0 | 0 | 1921 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:380-380 Manjunatha KR; Chettn GK; Arathi R; Bhaskar RG; Nandini PM; Chandra S; Bhaskaran GS; Brahmachari V Fragile-X syndrome: Cytogenetics and molecular analysis of subjects from Indian population | 0 | 0 |
| 2243 | 0 | 0 | 1922 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:405-405 Munir F; Comish KM; Wilding J A neuropsychological profile of attention and hyperactivity in boys with fragile-X syndrome: Implications for clinical intervention | 0 | 0 |
| 2244 | 0 | 0 | 1923 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:419-419 Orsmond G; Abbeduto L; Pavetto M; O'Brien A; Kesin E; Weissman M; Karadottir S; Cawthon S Stress and coping in parents of adolescents and young adults with fragile-X syndrome or Down syndrome | 0 | 0 |
| 2245 | 0 | 0 | 1924 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:449-449 Sabaratnam M; Murthy V; Wijeratne A Fragile-X syndrome: A 10-year follow-up | 0 | 0 |
| 2246 | 0 | 0 | 1925 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:483-483 Tassone F; Hagerman RJ; Loesch DZ; Lachiewicz A; Taylor AK; Hagerman PJ FMRI messenger RNA levels in male subjects with fragile-X syndrome | 0 | 0 |
| 2247 | 0 | 0 | 1926 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:496-497 Tzeng CC; Lin SJ; Chen YY; Chen RM An effective strategy of using a molecular test to screen individuals with mental retardation for fragile-X syndrome | 0 | 0 |
| 2248 | 0 | 0 | 1927 2000 JOURNAL OF INVESTIGATIVE MEDICINE 48(1):11A-11A Peterson TL; Hagerman RJ; Tassone F Genotype-phenotype relationships in fragile X families. | 0 | 0 |
| 2249 | 0 | 0 | 1928 2000 JOURNAL OF MEDICAL GENETICS 37:S18-S18 Mandel JL The fragile X syndrome: from families to CGG expansions and FMR1 gene function | 0 | 0 |
| 2250 | 0 | 0 | 1929 2000 JOURNAL OF MEDICAL GENETICS 37:S20-S20 Fisher A; Macpherson JN; Dennis NR; Barber JCK Targeted testing for fragile X: an audit of the first year. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2251 | 0 | 0 | 1930 2000 JOURNAL OF MEDICAL GENETICS 37:S44-S44 James T; Trigg A; Lindley VH; Fews GA; Roberts E; McKeown C; Davison EV An unexpected finding of fragile X (FRAXA) syndrome in a fetal blood sample referred for abnormalities on ultrasound scan | 0 | 0 |
| 2252 | 0 | 0 | 1931 2000 JOURNAL OF MEDICAL GENETICS 37:S66-S66 Lazarou LP; Myring J; Knight SJL; Gardner AP; Clarke A Fragile X (E) syndrome. How common is it? | 0 | 0 |
| 2253 | 0 | 0 | 1932 2000 JOURNAL OF MEDICAL GENETICS 37:S75-S75 Fratter C; Morsman A; Seller A Genetic analysis for Fragile X syndrome by fluorescent PCR | 0 | 0 |
| 2254 | 0 | 0 | 1933 2000 JOURNAL OF MEDICAL GENETICS 37:S78-S78 Chotai K; Buckingham AE; Bentley CM; Wycherley RJ; Payne SJ Fragile-X intermediate alleles - A clinical dilemma | 0 | 0 |
| 2255 | 0 | 0 | 1965 2001 ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY 221:U3-U3 Rodesittisuk P; Romero RM; Haworth IS Conformation of fragile X-associated triplet repeat DNA containing C-C mismatch pairs. | 0 | 0 |
| 2256 | 0 | 0 | 1968 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):177-177 Hagerman RJ; Greco C; Chudley A; Leehey M; Tassone F; Grigsby J; Hills J; Wilson R; Harris SW; Hagerman PJ Neuropathology and neurodegenerative features in some older male premutation carriers of fragile X syndrome. | 3 | 4 |
| 2257 | 0 | 0 | 1969 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 |
| 2258 | 0 | 0 | 1970 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 |
| 2259 | 0 | 0 | 1971 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 |
| 2260 | 0 | 0 | 1972 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2261 | 0 | 0 | 1973 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):431-431 Jenkins EC; Li SY; Yao XL; Lanter S; Sudhalter V; Belser R; Ding XH; Houck GE; Glicksman A; Dobkin CS; Nolin SL; Brown WT Detecting mosaic FMR-1 (fragile X) mutations: Southern blotting versus monoclonal antibody analysis. | 0 | 0 |
| 2262 | 0 | 0 | 1974 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):436-436 Patel ZM; Menon SR; D'souza AK; Adhia RA; Sanghavi DA; Gawde HM Validity of the analysis of FMRP expression in blood smears as a screening method for the fragile X syndrome in Indian population. | 0 | 0 |
| 2263 | 0 | 0 | 1975 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 |
| 2264 | 0 | 0 | 1976 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):554-554 Heine-Sur D; Pico G; Torres-Juan L; Bernues M; Iglesias J; Barcelo F; Rosell J A female with Fragile-X shows an affected male-like phenotype and skewed inactivation of the functional chromosome. | 0 | 0 |
| 2265 | 0 | 0 | 1977 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 |
| 2266 | 0 | 0 | 1978 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 |
| 2267 | 0 | 0 | 1979 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 |
| 2268 | 0 | 0 | 1980 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):667-667 Brown WT; Nolin S; Houck GE; Ding XH; Glicksman A; Li SH; Brooks S; Dobkin C; Jenkins EC The Fragile X Syndrome: Screening and prenatal diagnosis. | 0 | 0 |
| 2269 | 0 | 0 | 1981 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):669-669 Mallolas J; Badenas C; Rite M; Soler A; Borrell A; Sanchez A; Mila M Prospective study of molecular fragile X syndrome prenatal diagnosis. | 0 | 0 |
| 2270 | 0 | 0 | 1989 2001 AMERICAN JOURNAL OF MEDICAL GENETICS 105(7):585-585 Daly E; Moore CJ; Schmitz N; Jacobs PA; Davis KE; Murphy KC; Murphy DGM Premutation expansion of CGG triplet repeats affects brain; A study of male carriers of Fragile X syndrome | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2271 | 0 | 0 | 1997 2001 ANNALS OF NEUROLOGY 50(3):S108-S108 Berry-Kravis E Characterization of epilepsy in fragile X syndrome | 0 | 0 |
| 2272 | 0 | 0 | 1999 2001 AUSTRALIAN JOURNAL OF PSYCHOLOGY 53(1):58-58 Gould E Melatonin profiles and sleep characteristics in boys with fragile X Syndrome: A preliminary study | 0 | 0 |
| 2273 | 0 | 0 | 2030 2001 JOURNAL OF DENTAL RESEARCH 80(4):1133-1133 Sabbagh A Clinical and panoramic radiographic considerations of oral conditions in Fragile X Syndrome (Martin-Bell Syndrome) | 0 | 0 |
| 2274 | 0 | 0 | 2036 2001 JOURNAL OF MEDICAL GENETICS 38:S39-S39 Moore C; Daly EM; Tassone F; Schmitz N; Hagerman P; Jacobs P; Davies K; Murphy KC; Murphy DGM Neuroanatomical effect of FMR1 gene mRNA in premutation carriers of Fragile X syndrome | 0 | 0 |
| 2275 | 0 | 0 | 2037 2001 JOURNAL OF MEDICAL GENETICS 38:S40-S40 Daly E; Moore CJ; Schmitz N; Jacobs P; Davies K; Murphy KC; Murphy DGM Premutation expansion of CGG triplet repeats affects brain; a study of Male Carriers of Fragile X Syndrome | 0 | 0 |
| 2276 | 0 | 0 | 2038 2001 JOURNAL OF MEDICAL GENETICS 38:S63-S63 Warburton S; Waters J; Davison V Targeted diagnostic testing for fragile X syndrome | 0 | 0 |
| 2277 | 0 | 0 | 2039 2001 JOURNAL OF MEDICAL GENETICS 38:S64-S64 Wakeling W; King W; Taylor R Chemiluminescence detection offers a safe, effective and convenient alternative to radioisotopic labelling of probes for detection of Fragile X syndrome and other single gene disorders | 0 | 0 |
| 2278 | 0 | 0 | 2046 2001 NEUROIMAGE 13(6):S1076-S1076 Moore CJ; Daly EM; Schmitz N; Murphy KC; Murphy DGM Premutation expansion of CGG triplet repeats affects brain; a study of male carriers of Fragile X syndrome | 0 | 0 |
| 2279 | 0 | 0 | 2072 2001 REVISTA DE NEUROLOGIA 33:S88-S90 [Anon] Interdisciplinary conference on the fragile X syndrome - Barcelona, October 27-28, 2001 - Abstracts | 0 | 0 |
| 2280 | 0 | 0 | 2073 2001 SCIENCE 294(5548):1809-1809 Sohn E Genetics - Fragile X's missing partners identified | 0 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2281 | 0 | 0 | 2078 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):175-175 Jin P; Zhang F; Zarnescu DC; Moses K; Lucchesi JC; Nichol K; Pearson CE; Warren ST A Drosophila model of fragile X premutation: CGG repeat instability and dominant-negative effects of premutation riboCGG repeat. | 0 | 0 |
| 2282 | 0 | 0 | 2079 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):185-185 Jacquemont S; Hagerman RJ; Leehey M; Greco C; Brunberg J; Tassone F; Gane LW; Jardini T; Harris SW; Zhang L; Grigsby J; Des Portes V; Berry-Kravis E; Brown WT; Hagerman PJ Characterization of a progressive neurological condition in older adult male carriers of the fragile X premutation. | 2 | 2 |
| 2283 | 0 | 0 | 2080 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):259-259 Hagerman PJ; Greco CM; Hagerman RJ; Tassone F; Chudley AE; Del Bigio R; Jacquement S; Gane L; Leehey M Neuronal intranuclear inclusions in a tremor/ataxia syndrome among fragile X premutation carriers. | 0 | 0 |
| 2284 | 0 | 0 | 2081 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):270-270 Griffin KJ; Bei T; Meck J; Wong LJ; Bondy C; Stratakis CA Gender ambiguity and fragile X: a new syndrome. | 0 | 0 |
| 2285 | 0 | 0 | 2082 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):287-287 Hagerman R; Goodlin-Jones BL; Spence S; Albrect L; Bacalman S; Tassone F; Gane LW; Harris SW; Hagerman PJ The fragile X premutation and autistic spectrum disorders. | 0 | 0 |
| 2286 | 0 | 0 | 2083 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):288-288 Harris SW; Goodlin-Jones BL; Bacalman S; Jardini T; Rao S; Hagermann RJ Fragile X and autism diagnosis by two standard methodologies. | 0 | 0 |
| 2287 | 0 | 0 | 2084 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 |
| 2288 | 0 | 0 | 2085 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):347-347 Brown WT; Nolin SL; Dobkin CS; Houck GS; Glicksman A; Ding XD; Gargano AD; Crawford L; Gitcho N; Spence SJ; Geschwind DH; Agre Frequency of fragile X in multiplex autism: Testing the AGRE families. | 0 | 0 |
| 2289 | 0 | 0 | 2086 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 |
| 2290 | 0 | 0 | 2087 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):377-377 Zabala WM; Nava N; Gonzalez S; Delgado W; Borjas L; Fernandez E; Rojas A; Pineda L Clinical and molecular analysis of the fragile X syndrome in mentally retarded males from the Venezuelan northwestern region. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2291 | 0 | 0 | 2088 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 |
| 2292 | 0 | 0 | 2089 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):505-505 Dobkin CS; Ding XH; Houck GE; Mitchell E; Brown WT; Nolin SL A rare Eag I polymorphism that may confound fragile X diagnosis. | 0 | 0 |
| 2293 | 0 | 0 | 2090 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 |
| 2294 | 0 | 0 | 2091 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 |
| 2295 | 0 | 0 | 2092 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):523-523 Bastaki LA; Al-Awadi SA; Hegazi FA; Turky NA; Mustafa MA; Naguib KA PCR technique and significance in fragile X syndrome. | 0 | 0 |
| 2296 | 0 | 0 | 2101 2002 AMERICAN JOURNAL OF MEDICAL GENETICS 114(7):833-833 Steyaert J; Borghgraef M; Fryns JP A distinct neurocognitive phenotype in female fragile X premutation carriers | 0 | 0 |
| 2297 | 0 | 0 | 2105 2002 ANNALS OF NEUROLOGY 52(3):S86-S86 Berry-Kravis E; Lewin F; Wuu J; Leehey M; Hagerman R; Hagerman P; Goetz C Tremor and ataxia in adult fragile X premutation carriers: Blinded videotape evaluation | 0 | 0 |
| 2298 | 0 | 0 | 2122 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:55-56 Carmichael B Fragile X Syndrome - its impact on families | 0 | 0 |
| 2299 | 0 | 0 | 2123 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:63-63 Hagerman PJ; Greco CM; Tassone F; Chudley A; Del Bigio MR; Jacquemont S; Leehey M; Hagerman RJ Neuronal intranuclear inclusions in a new cerebellar tremor/ataxia syndrome among fragile X carriers | 0 | 0 |
| 2300 | 0 | 0 | 2124 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:220-220 Loesch DZ Effect of prennutation in the FMR1 gene on cognitive and physical phenotype in fragile X assessed by pedigree analysis. | 0 | 0 |
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