| Missing Links? Citation Matrix | Graphs | Glossary HistCite Guide About |
Nodes: 2647,
Authors: 5321,
Journals: 428,
Outer References: 16458,
Words: 3536
Collection span: 1967 - 2005
View: Overview. Sorted by GCS.
Page 9: 1 2 3 4 5 6 7 8 9
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 2401 | 8 | 25 | 2199 2001 REVISTA DE NEUROLOGIA 33:S20-S23 Mila M; Mallolas J Fragile X syndrome: Premature ovarian failure. Preimplantation and preconception genetic diagnosis | 0 | 0 |
| 2402 | 3 | 19 | 2202 2001 REVISTA DE NEUROLOGIA 33:S32-S36 Goldson E Sensory integration and fragile X syndrome | 0 | 0 |
| 2403 | 2 | 12 | 2203 2001 REVISTA DE NEUROLOGIA 33:S37-S41 Carrasco M Informing members of families affected by fragile X syndrome of this diagnosis | 0 | 0 |
| 2404 | 15 | 42 | 2204 2001 REVISTA DE NEUROLOGIA 33:S41-S50 Artigas-Pallares J; Brun-Gasca C Medical treatment of fragile X syndrome | 0 | 0 |
| 2405 | 63 | 105 | 2205 2001 REVISTA DE NEUROLOGIA 33:S51-S57 Hagerman RJ; Hagerman PJ Fragile X syndrome: A model of gene-brain-behaviour relationships | 0 | 0 |
| 2406 | 14 | 29 | 2206 2001 REVISTA DE NEUROLOGIA 33:S62-S65 Chiurazzi P; Neri G Experimental therapy: Reactivation of the FMR1 gene involved in fragile X syndrome | 0 | 0 |
| 2407 | 3 | 52 | 2207 2001 REVISTA DE NEUROLOGIA 33:S65-S70 Calvani M; D'Iddio S; de Gaetano A; Mariotti P; Mosconi L; et al. L-acetylcarnityne treatment on fragile X patients hyperactive behaviour | 0 | 0 |
| 2408 | 9 | 40 | 2208 2001 REVISTA DE NEUROLOGIA 33:S70-S76 de Diego-Otero Y Experimental therapeutic models for fragile X syndrome | 0 | 0 |
| 2409 | 0 | 7 | 2209 2001 REVISTA DE NEUROLOGIA 33:S77-S81 Safont-Tria NB Psychomotricity and fragile X syndrome | 0 | 0 |
| 2410 | 0 | 7 | 2210 2001 REVISTA DE NEUROLOGIA 33:S82-S87 Furgang R Language therapy in fragile X syndrome | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2411 | 0 | 0 | 2211 2001 REVISTA DE NEUROLOGIA 33:S88-S90 [Anon] Interdisciplinary conference on the fragile X syndrome - Barcelona, October 27-28, 2001 - Abstracts | 0 | 0 |
| 2412 | 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 |
| 2413 | 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 |
| 2414 | 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 |
| 2415 | 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 |
| 2416 | 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 |
| 2417 | 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 |
| 2418 | 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 |
| 2419 | 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 |
| 2420 | 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 |
| 2421 | 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 |
| 2422 | 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 |
| 2423 | 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 |
| 2424 | 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 |
| 2425 | 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 |
| 2426 | 12 | 32 | 2237 2002 AMERICAN JOURNAL OF MEDICAL GENETICS 110(1):36-44 McConkie-Rosell A; Spiridigliozzi GA; Sullivan JA; Dawson DV; Lachiewicz AM Carrier testing in fragile X syndrome: When to tell and test | 0 | 0 |
| 2427 | 0 | 0 | 2242 2002 AMERICAN JOURNAL OF MEDICAL GENETICS 114(7):832-832 Moore CJ; Daly EM; Tassone F; Tysoe C; Schmitz N; et al. The effect of premutation CGG trinucleotide repeat expansion, and expression of FMR-1 protein, on brain anatomy | 0 | 0 |
| 2428 | 0 | 0 | 2243 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 |
| 2429 | 17 | 42 | 2246 2002 AMERICAN JOURNAL OF SPEECH-LANGUAGE PATHOLOGY 11(4):295-304 Roberts JE; Mirrett P; Anderson K; Burchinal M; Neebe E Early communication, symbolic behavior, and social profiles of young males with fragile X syndrome | 0 | 0 |
| 2430 | 0 | 0 | 2247 2002 ANNALS OF NEUROLOGY 52(3):S86-S86 Berry-Kravis E; Lewin F; Wuu J; Leehey M; Hagerman R; et al. Tremor and ataxia in adult fragile X premutation carriers: Blinded videotape evaluation | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2431 | 17 | 30 | 2250 2002 ARQUIVOS DE NEURO-PSIQUIATRIA 60(4):981-985 Yonamine SM; da Silva AA Characteristics of the communication in individuals with fragile X syndrome | 0 | 0 |
| 2432 | 0 | 0 | 2264 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:55-56 Carmichael B Fragile X Syndrome - its impact on families | 0 | 0 |
| 2433 | 0 | 0 | 2265 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:63-63 Hagerman PJ; Greco CM; Tassone F; Chudley A; Del Bigio MR; et al. Neuronal intranuclear inclusions in a new cerebellar tremor/ataxia syndrome among fragile X carriers | 0 | 0 |
| 2434 | 0 | 0 | 2266 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:220-220 Afifi HH; Abdel-Aleem AK; Shaheen OO Fragile X syndrome: clinical and behavioral study. | 0 | 0 |
| 2435 | 0 | 0 | 2267 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 |
| 2436 | 0 | 0 | 2268 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:227-227 Steinbach P; Jakubiczka S; Bettecken T X inactivation and fragile X methylation in human placentas | 0 | 0 |
| 2437 | 0 | 0 | 2269 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:228-228 Tzeng C; Chen W; Huang K Prevalence of fragile-X female carrier in Taiwan is lower than expected | 0 | 0 |
| 2438 | 0 | 0 | 2270 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:228-229 Biancalana V; Beldjord C; de Martinville B; Bieth E; Blayau M; et al. 5 years of molecular diagnosis of Fragile X syndrome (1997-2001): a collaborative study of 22 laboratories in France. | 0 | 0 |
| 2439 | 0 | 0 | 2271 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:229-229 Deelen WH; Jansen C; Ramlakhan SR; Labrijn-Marks I; Olmer R; et al. Five years experience with DIG labeled probes on Southern blots applied in Fragile X diagnostics | 0 | 0 |
| 2440 | 0 | 0 | 2272 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:229-229 Hasanzad M; Amini SH; Taghizadeh F; Teimourian S; Karimi-Nejad R; et al. Analysis of FMR 1 methylation in Fragile X syndrome in Iranian population | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2441 | 0 | 0 | 2273 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:229-229 Gryschenko NV; Malarchuk SG; Livshits LA CGG-repeat expansion and metilation status of the promotor region of FMR1 gene analysis in the Fragile-X sindrome patients from Ukraine | 0 | 0 |
| 2442 | 0 | 0 | 2274 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:231-231 Zalfa F; Primerano B; Lauro C; Giorgi M; Moro A; et al. Towards an understanding of the Fragile X syndrome: FMRP is translated at the synapses where it acts as a translational regulator | 0 | 0 |
| 2443 | 0 | 0 | 2275 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:231-231 Gantois I; Reyniers E; Kooy F Differential gene expression in the fragile X mouse model | 0 | 0 |
| 2444 | 2 | 2 | 2276 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:231-231 Bardoni B; Schenck A; van de Bor V; Giangrande A; Mandel J Drosophila as a model to study the physiological pathway in which FMRP (Fragile X Mental Retardation Protein) is involved | 0 | 0 |
| 2445 | 0 | 0 | 2277 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:231-232 Pietrobono R; Pomponi MG; Tabolacci E; Oostra B; Chiurazzi P; et al. Quantitative analysis of DNA demethylation and trascriptional reactivation of the FMR1 gene in fragile X cells treated with 5-azadeoxycytidine | 0 | 0 |
| 2446 | 0 | 0 | 2278 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:232-232 McKelvie KB; Reynolds A; Tassone F; Taylor AK; Hagerman RJ Evidence for skewed X chromosome inactivation in females with the fragile X full mutation | 0 | 0 |
| 2447 | 0 | 0 | 2279 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:323-323 Wilson R; Epstein JH; McKelvie K; Grisgby J; Nagamoto H; et al. Psychological and neuropsychological findings in adults with the premutation and full mutation for Fragile X Syndrome | 0 | 0 |
| 2448 | 0 | 0 | 2280 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:323-323 O'Connor R; Riley K; Epstein J; Wilson R; McKelvie K; et al. Analysis of ADHD subtypes in Fragile X syndrome | 0 | 0 |
| 2449 | 0 | 0 | 2283 2002 GENETIC COUNSELING 13(2):207-261 [Anon] Abstracts of the 10th International Workshop on Fragile X and X-Linked Mental Retardation - 19-22 September 2001, Frascati, Italy | 0 | 0 |
| 2450 | 31 | 49 | 2284 2002 GENETICS AND MOLECULAR BIOLOGY 25(1):1-6 de Diego Y; Hmadcha A; Moron F; Lucas M; Carrasco M; et al. Fragile X founder effect and distribution of CGG repeats among the mentally retarded population of Andalusia, South Spain | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2451 | 19 | 33 | 2285 2002 GENOMICS 80(2):151-157 Baskaran S; Datta S; Mandal A; Gulati N; Totey SM; et al. Instability of CGG repeats in transgenic mice | 0 | 0 |
| 2452 | 2 | 3 | 2290 2002 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 32(1):60-61 Rapin I Legitimacy of comparing fragile X with autism questioned | 0 | 0 |
| 2453 | 0 | 0 | 2296 2002 JOURNAL OF COGNITIVE NEUROSCIENCE :50-51 Scerif G; Wilding J; Cornish K; Driver J; Humphreys K; et al. Executive control in visual search for multiple targets in toddlers with Fragile X Syndrome | 0 | 0 |
| 2454 | 0 | 0 | 2300 2002 JOURNAL OF MEDICAL GENETICS 39:S73-S73 Bilgen T; Keser I; Mihci E; Tacoy S; Haspolat S; et al. Screening of the FMR1 gene (CCG)n expansion by expand long PCR in families with fragile X syndrome in antalya province. | 0 | 0 |
| 2455 | 0 | 0 | 2301 2002 JOURNAL OF MEDICAL GENETICS 39:S76-S76 Jani A; Hodsdon P; Churchley K; Crocker M; Stefanou E; et al. An atypical week for the Oxford Fragile X service: Two interesting cases | 0 | 0 |
| 2456 | 18 | 20 | 2302 2002 JOURNAL OF MEDICAL GENETICS 39(3):196-200 Tarleton J; Kenneson A; Taylor AK; Crandall K; Fletcher R; et al. A single base alteration in the CGG repeat region of FMR1: possible effects on gene expression and phenotype | 0 | 0 |
| 2457 | 0 | 0 | 2303 2002 JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY 61(5):450-450 Greco CM; Hagerman RJ; Tassone F; Chudley AE; Del Bigio MR; et al. Neuronal and astrocytic intranuclear inclusions in Fragile X carriers with cerebellar tremor/ataxia and cognitive changes. | 0 | 0 |
| 2458 | 0 | 0 | 2307 2002 LANCET NEUROLOGY 1(3):141-141 May TS Evidence of altered synaptic plasticity found in fragile X syndrome | 0 | 0 |
| 2459 | 10 | 14 | 2312 2002 MICROSCOPY RESEARCH AND TECHNIQUE 57(3):156-158 Churchill JD; Beckel-Mitchener A; Weiler IJ; Greenough WT Effects of fragile X syndrome and an FMR1 knockout mouse model on forebrain neuronal cell biology | 0 | 0 |
| 2460 | 35 | 66 | 2320 2002 MONATSSCHRIFT KINDERHEILKUNDE 150(12):1486-+ Backes M; von Gontard A Behavioural phenotype of fragile X syndrome | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2461 | 8 | 16 | 2322 2002 NATURE MEDICINE 8(11):1204-1205 Hansen RS; Laird CD A new regulatory pathway for fragile X syndrome? | 0 | 0 |
| 2462 | 2 | 3 | 2323 2002 NATURE REVIEWS GENETICS 3(1):4-5 Patterson M Twin-track approach to fragile X | 0 | 0 |
| 2463 | 0 | 0 | 2327 2002 NEUROLOGY 58(6):987-987 Munoz DG Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X | 0 | 0 |
| 2464 | 0 | 0 | 2328 2002 NEUROLOGY 58(6):987-988 Hagerman RJ; Greco C; Jacquemont S; Leehy M; Hagerman P Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X - Reply | 0 | 0 |
| 2465 | 0 | 0 | 2329 2002 NEUROLOGY 58(7):A481-A482 Leehey MA; Brunberg JA; Lang AE; Jacquemont S; Rubinstein D; et al. MRI increased T2 signal intensity in the cerebellar peduncles: Specific for the fragile X premutation tremor/ataxia syndrome? | 0 | 0 |
| 2466 | 0 | 0 | 2330 2002 NEUROLOGY 58(7):A482-A482 Munhoz RP; Lozano AM; Lang AE Fragile X syndrome premutation mistaken as essential tremor: An unrecognized source of diagnostic confusion | 0 | 0 |
| 2467 | 0 | 0 | 2337 2002 ONKOLOGIE 25(5):482-483 Diel I; Chatsiproios D Concept of integrated gyneco-oncological care: Centrum fur ganzheitliche gynakologie (CGG Klinik GmbH) | 0 | 0 |
| 2468 | 13 | 27 | 2339 2002 PEDIATRICS 109(1) Flynn BJ; Myers SM; Cera PJ; Mowad JJ Testicular torsion in an adolescent with fragile X syndrome | 0 | 0 |
| 2469 | 0 | 0 | 2346 2002 SCIENTIST 16(20):8-8 Johnston N Fragile X, an RNAi connection? | 0 | 0 |
| 2470 | 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 |
| 2471 | 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 |
| 2472 | 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 |
| 2473 | 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 |
| 2474 | 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 |
| 2475 | 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 |
| 2476 | 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 |
| 2477 | 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 |
| 2478 | 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 |
| 2479 | 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 |
| 2480 | 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 |
| 2481 | 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 |
| 2482 | 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 |
| 2483 | 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 |
| 2484 | 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 |
| 2485 | 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 |
| 2486 | 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 |
| 2487 | 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 |
| 2488 | 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 |
| 2489 | 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 |
| 2490 | 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 |
| 2491 | 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 |
| 2492 | 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 |
| 2493 | 6 | 8 | 2374 2003 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 116A(1):99-100 Banes SL; Begleiter ML; Butler MG 45,X/46,XY mosaicism and fragile X syndrome | 0 | 0 |
| 2494 | 11 | 18 | 2375 2003 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 116A(2):176-178 Stalker HJ; Keller KL; Gray BA; Zori RT Concurrence of fragile X syndrome and 47, XYY in an individual with a Prader-Willi-Like phenotype | 0 | 0 |
| 2495 | 0 | 0 | 2384 2003 AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY 189(6):S117-S117 Musci TJ; Caughey AB Cost-effectiveness analysis of prenatal population-based fragile X carrier screening | 0 | 0 |
| 2496 | 10 | 21 | 2388 2003 ANNALES DE GENETIQUE 46(1):53-55 Santos CB; Hjalgrim H; Carneiro FRG; Ribeiro M; Boy RT; et al. Concurrence of fragile X and Klinefelter syndromes: report of a new case of paternal nondisjunction | 0 | 0 |
| 2497 | 0 | 0 | 2391 2003 ANNALS OF NEUROLOGY 54:S144-S144 Berry-Kravis E; Potanos K Clinical response to psychopharmacology for behavior in Fragile X syndrome | 0 | 0 |
| 2498 | 0 | 0 | 2392 2003 ANNALS OF NEUROLOGY 54:S150-S150 Berry-Kravis E; Potanos K Stimulant therapy in fragile X syndrome | 0 | 0 |
| 2499 | 11 | 15 | 2393 2003 ARCHIVES DE PEDIATRIE 10(5):401-402 Ramos FJ; Willemsen R Diagnosis of the Fragile X Syndrome by the analysis of FMRP expression in blood and hair roots | 0 | 0 |
| 2500 | 2 | 12 | 2395 2003 ARCHIVES OF NEUROLOGY 60(9):1197-1200 Kalidas S; Smith DP Functional genomics, fragile X syndrome, and RNA interference | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2501 | 1 | 26 | 2396 2003 BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 303(1):81-90 Monleon D; Esteve V; Celda B NMR study of hexanucleotide d(CCGCGG)(2) containing two triplet repeats of fragile X syndrome | 0 | 0 |
| 2502 | 4 | 6 | 2400 2003 BIOFUTUR (229):36-37 Nourrit F Fragile X and interference. | 0 | 0 |
| 2503 | 0 | 0 | 2401 2003 BIOLOGICAL PSYCHIATRY 53(8):49S-49S Daly EM; Moore CJ; Schmitz N; Morris R; Murphy KC; et al. Expansion of CGG trinucleotide repeats: Effect on neuropsychology of male premutation carriers of Fragile X syndrome | 0 | 0 |
| 2504 | 0 | 0 | 2402 2003 BIOLOGICAL PSYCHIATRY 53(8):152S-152S Moore CJ; Daly EM; Tassone F; Tysoe C; Schmitz N; et al. The effect of premutation CGG trinucleotide repeat expansion, and %FMRP(+) lymphocytes reduction, on brain anatomy | 0 | 0 |
| 2505 | 0 | 1 | 2410 2003 CLINICAL GENETICS 64(2):106-108 Leavitt BR Something lost in the translation: 'premutations' in the FMR1 gene cause Fragile X tremor/ataxia syndrome (FXTAS) | 0 | 0 |
| 2506 | 43 | 136 | 2412 2003 CYTOGENETIC AND GENOME RESEARCH 100(1-4):65-76 Greene E; Handa V; Kumari D; Usdin K Transcription defects induced by repeat expansion: fragile X syndrome, FRAXE mental retardation, progressive myoclonus epilepsy type 1, and Friedreich ataxia | 0 | 0 |
| 2507 | 11 | 59 | 2414 2003 CYTOGENETIC AND GENOME RESEARCH 100(1-4):140-146 Fleming K; Riser DK; Kumari D; Usdin K Instability of the fragile X syndrome repeat in mice: the effect of age, diet and mutations in genes that affect DNA replication, recombination and repair proficiency | 0 | 0 |
| 2508 | 152 | 233 | 2417 2003 DEVELOPMENT AND PSYCHOPATHOLOGY 15(4):927-968 Reiss AL; Dant CC The behavioral neurogenetics of fragile X syndrome: Analyzing gene-brain-behavior relationships in child developmental psychopathologies | 0 | 0 |
| 2509 | 0 | 0 | 2418 2003 DEVELOPMENTAL BIOLOGY 259(2):528-529 Qin M; Kang J; Smith CB Increased local rates of cerebral protein synthesis in fragile X knockout mice. | 0 | 0 |
| 2510 | 28 | 34 | 2421 2003 GENETIC TESTING 7(4):303-308 Gasteiger M; Grasbon-Frod E; Neitzel B; Kooy F; Holinski-Feder E FMR1 gene deletion/reversion: A pitfall of fragile X carrier testing | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2511 | 3 | 7 | 2423 2003 GENETIC TESTING 7(4):345-346 Adir V; Shahak E; Dar H; Borochowitz ZU Detection of X chromosome aneuploidy using Southern blot analysis during routine population-based screening for Fragile X syndrome | 0 | 0 |
| 2512 | 28 | 41 | 2425 2003 HEREDITY 90(3):206-211 Arrieta I; Penagarikano O; Tele M; Ortega B; Flores P; et al. The FMR1 CGG repeat and linked microsatellite markers in two Basque valleys | 0 | 0 |
| 2513 | 21 | 29 | 2433 2003 HUMAN REPRODUCTION 18(8):1637-1640 Gersak K; Meden-Vrtovec H; Peterlin B Fragile X premutation in women with sporadic premature ovarian failure in Slovenia | 0 | 0 |
| 2514 | 45 | 118 | 2435 2003 INTERNATIONAL REVIEW OF RESEARCH IN MENTAL RETARDATION, VOL 27 27:83-119 Murphy MM; Abbeduto L Language and communication in fragile X syndrome | 0 | 0 |
| 2515 | 0 | 0 | 2439 2003 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 24(5):393-393 Hansen R; Goodlin-Jones B; Nowicki S; Heeren M; Herman K; et al. Behavioral phenotypes in older children with autistic spectrum disorders and fragile X: Similarities and differences | 0 | 0 |
| 2516 | 0 | 0 | 2440 2003 JOURNAL OF FORENSIC SCIENCES 48(5):1200-1200 Cotton RW; Word CJ Commentary on: Thompson WC, Taroni F, Aitken CGG. How the probability of a false positive affects the value of DNA evidence. J Forensic Sci 2003;48(1):47-54. | 0 | 0 |
| 2517 | 0 | 0 | 2441 2003 JOURNAL OF FORENSIC SCIENCES 48(5):1201-1201 Clarke GW Commentary on: Thompson WC, Taroni F, Aitken CGG. How the probability of a false positive affects the value of DNA evidence. J Forensic Sci 2003;48(1):47-54. | 0 | 0 |
| 2518 | 0 | 0 | 2442 2003 JOURNAL OF FORENSIC SCIENCES 48(5):1202-1202 Thompson WC; Taroni F; Aitken CGG Commentary on: Thompson WC, Taroni F, Aitken CGG. How the probability of a false positive affects the value of DNA evidence. J Forensic Sci 2003;48(1):47-54. Author's response | 0 | 0 |
| 2519 | 0 | 0 | 2444 2003 JOURNAL OF MEDICAL GENETICS 40:S15-S15 Ennis S; Collins A; Morton NE SNP-based haplotypes and LD blocks in the fragile X region | 0 | 0 |
| 2520 | 0 | 0 | 2445 2003 JOURNAL OF MEDICAL GENETICS 40:S49-S49 Dalton A; Mills AC; Rigby A; Manly T; Hollis C; et al. The neuropsychological phenotype of fragile X premutation males | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2521 | 0 | 0 | 2446 2003 JOURNAL OF MEDICAL GENETICS 40:S80-S80 Payne S; Powell CM Fragile-X intermediate alleles - instability and inconclusion | 0 | 0 |
| 2522 | 0 | 0 | 2449 2003 JOURNAL OF NEUROCHEMISTRY 85:1-1 Huber KM Recent progress in understanding the neural mechanisms of Fragile X Syndrome | 0 | 0 |
| 2523 | 19 | 35 | 2450 2003 JOURNAL OF NEUROGENETICS 17(2-3):223-230 Major T; Culjkovic B; Stojkovic O; Gucscekic M; Lakic A; et al. Prevalence of the fragile X syndrome in Yugoslav patients with non-specific mental retardation | 0 | 0 |
| 2524 | 0 | 0 | 2451 2003 JOURNAL OF PSYCHOSOMATIC RESEARCH 55(2):156-156 Mirzaei M; Karam GA; Mahmoudi M Evaluation of prevalence the fragile X syndrome in 52 patients with moderate mental retardation with cytogenetic methods. | 0 | 0 |
| 2525 | 8 | 10 | 2452 2003 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 42(3):372-375 Lombroso PJ Genetics of childhood disorders: XLVIII. Learning and memory, part 1: Fragile X syndrome update | 0 | 0 |
| 2526 | 21 | 28 | 2454 2003 JOURNAL OF THE FORMOSAN MEDICAL ASSOCIATION 102(1):12-16 Chi J; Chen DJ; Lin CN; Chiu CY; Huang CB; et al. Feasibility of blood spot PCR in large-scale screening of fragile X syndrome in southern Taiwan | 0 | 0 |
| 2527 | 23 | 69 | 2455 2003 LANGUAGE SPEECH AND HEARING SERVICES IN SCHOOLS 34(4):320-331 Mirrett PL; Roberts JE Early intervention practices and communication intervention strategies for young males with fragile X syndrome | 0 | 0 |
| 2528 | 0 | 0 | 2457 2003 MOVEMENT DISORDERS 18(9):1091-1091 Kraft S; Parboosingh J; Suchowersky O Absence of fragile X premutation alleles in patients referred with spinocerebellar ataxia | 0 | 0 |
| 2529 | 1 | 1 | 2458 2003 NATURE REVIEWS GENETICS 4(10):758-758 Casci T Fragile X: a class of its own | 0 | 0 |
| 2530 | 1 | 3 | 2459 2003 NATURE REVIEWS NEUROSCIENCE 4(4):245-245 Jones R Cell biology or the neuron - FMRP and its many partners | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2531 | 1 | 1 | 2460 2003 NATURE REVIEWS NEUROSCIENCE 4(10):776-777 Casci T Neurological disorders - Fragile X: a class of its own | 0 | 0 |
| 2532 | 1 | 1 | 2472 2003 PRENATAL DIAGNOSIS 23(9):771-771 Rife M; Mallolas J; Badenas C; Tazon B; Miguelez MR; et al. Pilot study for the neonatal screening of fragile X syndrome (vol 22, pg 459, 2002) | 0 | 0 |
| 2533 | 5 | 10 | 2479 2004 ACTA PHARMACOLOGICA SINICA 25(7):973-976 Sun YJ; Han X Dynamic behavior of fragile X full mutations in cultured female fetal fibroblasts | 0 | 0 |
| 2534 | 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 |
| 2535 | 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 |
| 2536 | 19 | 29 | 2485 2004 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 124A(2):129-132 Rife M; Nadal A; Mila M; Willemsen R Immunohistochemical FMRP studies in a full mutated female fetus | 0 | 0 |
| 2537 | 9 | 16 | 2486 2004 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 124A(2):213-215 Marshall I; Betensky BP; Goseco A; Vogiatzi MV; Flieder D Fragile x and mosaic 45,X/46,XY mixed gonadal dysgenesis in a girl with ambiguous genitalia | 0 | 0 |
| 2538 | 31 | 38 | 2489 2004 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 128A(3):250-255 Penagarikano O; Gil A; Telez M; Ortega B; Flores P; et al. A new insight into fragile X syndrome among Basque population | 0 | 0 |
| 2539 | 25 | 40 | 2490 2004 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 129A(2):184-189 Zeesman S; Zwaigenbaum L; Whelan DT; Hagerman RJ; Tassone F; et al. Paternal transmission of fragile X syndrome | 0 | 0 |
| 2540 | 24 | 59 | 2492 2004 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 129A(3):225-234 Kaufmann WE; Cortell R; Kau CSM; Bukelis I; Tierney E; et al. Autism spectrum disorder in fragile X syndrome: Communication, social interaction, and specific behaviors | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2541 | 11 | 16 | 2493 2004 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 129A(3):326-328 Clarke NF; Mowat D; Kooy RF; Reyniers E; Willemsen R Fragile X syndrome phenotype with normal FMR1 gene studies | 0 | 0 |
| 2542 | 0 | 0 | 2497 2004 ANNALS OF NEUROLOGY 56:S104-S104 Cortell R; Bukelis I; Gray RM; Cox C; Tierney E; et al. Autism spectrum disorder in boys with Fragile X: Serial evaluation | 0 | 0 |
| 2543 | 0 | 0 | 2499 2004 BEHAVIOR GENETICS 34(6):638-638 Fisch GS; Simensen RJ; Schroer RJ Longitudinal assessment of cognitive-behavioral features of children and adolescents with either autism or the fragile X mutation | 0 | 0 |
| 2544 | 0 | 0 | 2500 2004 BIOLOGICAL PSYCHIATRY 55:159S-159S Daly EM; Moore CJ; Simmons A; Tassone F; Tysoe C; et al. A H-1 magnetic resonance spectroscopy study of males with premutation expansion of CGG trinucleoticle repeats | 0 | 0 |
| 2545 | 23 | 40 | 2502 2004 BRAIN 127:2672-2681 Moore CJ; Daly EM; Tassone F; Tysoe C; Schmitz N; et al. The effect of pre-mutation of X chromosome CGG trinucleotide repeats on brain anatomy | 0 | 0 |
| 2546 | 12 | 21 | 2503 2004 BRAIN & DEVELOPMENT 26(6):380-383 Suwa K; Momoi MY Non-invasive screening of fragile X syndrome A using urine and hair roots | 0 | 0 |
| 2547 | 3 | 6 | 2504 2004 BRAIN AND COGNITION 54(3):235-239 Cornish K; Swainson R; Cunnington R; Wilding J; Morris P; et al. Do women with fragile X syndrome have problems in switching attention: Preliminary findings from ERP and fMRI | 0 | 0 |
| 2548 | 0 | 0 | 2505 2004 BRAIN AND COGNITION 56(1):121-121 Kogan C; Boutet I; Cornish K; Andermann E; DerKaloustian V; et al. Evidence for a transient channel visual deficit in Fragile X Syndrome | 0 | 0 |
| 2549 | 51 | 120 | 2507 2004 CNS DRUGS 18(11):687-703 Tsiouris JA; Brown WT Neuropsychiatric symptoms of fragile X syndrome - Pathophysiology and pharmacotherapy | 0 | 0 |
| 2550 | 24 | 47 | 2508 2004 COGNITIVE NEUROPSYCHOLOGY 21(6):579-596 Keenan JM; Simon JA Inference deficits in women with Fragile X Syndrome: A problem in working memory | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2551 | 16 | 38 | 2511 2004 CYTOGENETIC AND GENOME RESEARCH 105(2-4):448-454 Errijgers V; Kooy RF Genetic modifiers in mice: the example of the fragile X mouse model | 0 | 0 |
| 2552 | 11 | 19 | 2515 2004 EUROPEAN JOURNAL OF OBSTETRICS GYNECOLOGY AND REPRODUCTIVE BIOLOGY 112(2):189-191 Bussani C; Papi L; Sestini R; Baldinotti F; Bucciantini S; et al. Premature ovarian failure and fragile X premutation: a study on 45 women | 0 | 0 |
| 2553 | 35 | 49 | 2516 2004 EXPERIMENTAL NEUROLOGY 189(2):343-353 Schrier M; Severijnen LA; Reis S; Rife M; van't Padje S; et al. Transport kinetics of FMRP containing the I304N mutation of severe fragile X syndrome in neurites of living rat PC12 cells | 0 | 0 |
| 2554 | 0 | 0 | 2517 2004 FERTILITY AND STERILITY 82:S246-S247 Malcov M; Carmon A; Mey-Raz N; Ben Yosef D; Lessing JB; et al. Preimplantation genetic diagnosis for fragile X syndrome in Israel | 0 | 0 |
| 2555 | 21 | 34 | 2518 2004 GENE 343(2):231-238 Guduric-Fuchs J; Mohrlen F; Frohme M; Frank U A fragile X mental retardation-like gene in a cnidarian | 0 | 0 |
| 2556 | 0 | 0 | 2520 2004 GENETIC COUNSELING 15(2):239-286 [Anon] Abstracts of the 11(th) International Workshop on Fragile X and X-Linked Mental Retardation - 27-30 August 2003, Pafos, Cyprus | 0 | 0 |
| 2557 | 27 | 42 | 2521 2004 GENETIC EPIDEMIOLOGY 26(4):294-304 Huggins RM; Loesch DZ; Qian GQ; Bui QM; Mitchell RJ; et al. Hierarchical Bayes model for random haplotype and family effects in the transmission of fragile-X | 0 | 0 |
| 2558 | 0 | 0 | 2522 2004 GENETICS IN MEDICINE 6(4):300-300 MacKenzie JJ; Sumargo IV; Taylor SA A cryptic full mutation in a male with a classical fragile X phenotype. | 0 | 0 |
| 2559 | 0 | 0 | 2523 2004 GENETICS IN MEDICINE 6(4):352-352 Han X; Chehab F; Powell B; Phalin-Rague J A high mental functioning fragile X male with a de novo 103bp deletion including entire CGG repeat region in > 50% of his peripheral leukocytes. | 0 | 0 |
| 2560 | 3 | 40 | 2525 2004 GENOMICS 84(1):69-81 Sarafidou T; Kahl C; Martinez-Garay I; Mangelsdorf M; Gesk S; et al. Folate-sensitive fragile site FRA10A is due to an expansion of a CGG repeat in a novel gene, FRA10AC1, encoding a nuclear protein | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2561 | 32 | 55 | 2526 2004 GROWTH HORMONE & IGF RESEARCH 14:S158-S165 Mandel JL; Biancalana V Fragile X mental retardation syndrome: from pathogenesis to diagnostic issues | 0 | 0 |
| 2562 | 0 | 9 | 2527 2004 HEMOGLOBIN 28(3):173-176 Regtuijt ME; Harteveld CL; Van Delft P; Akkermans N; Giordano PC Hb Suan-Dok [alpha 109(G16)Leu -> Arg; CTG--> CGG (alpha 2)] - Described in a patient of African ancestry | 0 | 0 |
| 2563 | 1 | 5 | 2530 2004 ISRAEL JOURNAL OF PSYCHIATRY AND RELATED SCIENCES 41(1):70-70 Kandil ST; Bilici M; Aksu HB; Celep F; Karaguzel A Early infantile autism and fragile X anomaly | 0 | 0 |
| 2564 | 1 | 1 | 2532 2004 JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION 291(24):2945-2945 Barrett SK; Drazin T; Rosa D; Kupchik GS Genetic counseling for families of patients with fragile X syndrome | 0 | 0 |
| 2565 | 1 | 1 | 2534 2004 JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION 292(17):2086-2086 Hagerman P Genetic counseling for families of patients with fragile X syndrome (vol 291, pg 2945, 2004) | 0 | 0 |
| 2566 | 60 | 103 | 2536 2004 JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY 45(6):1042-1053 Cornish KM; Turk J; Wilding J; Sudhalter V; Munir F; et al. Annotation: Deconstructing the attention deficit in fragile X syndrome: a developmental neuropsychological approach | 0 | 0 |
| 2567 | 22 | 57 | 2537 2004 JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM 89(9):4569-4574 Welt CK; Smith PC; Taylor AE Evidence of early ovarian aging in fragile X premutation carriers | 0 | 0 |
| 2568 | 6 | 36 | 2539 2004 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 25(1):21-27 Mirrett PL; Bailey DB; Roberts JE; Hatton DD Developmental screening and detection of developmental delays in infants and toddlers with fragile X syndrome | 0 | 0 |
| 2569 | 30 | 54 | 2540 2004 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 25(6):392-398 Goodlin-Jones BL; Tassone F; Gane LW Autistic spectrum disorder and the fragile X premutation | 0 | 0 |
| 2570 | 0 | 1 | 2541 2004 JOURNAL OF FORENSIC SCIENCES 49(1):192-193 Brenner CH; Inman K Commentary on: Thompson WC, Taroni F, Aitken CGG. How the probability of a false positive affects the value of DNA evidence. J Forensic Sci 2003;48(1): 47-54. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2571 | 0 | 3 | 2542 2004 JOURNAL OF FORENSIC SCIENCES 49(1):194-195 Thompson WC; Taroni PF; Aitken CGG 'Commentary on: Thompson WC, Taroni F, Aitken CGG. How the probability of a false positive affects the value of DNA evidence. J Forensic Sci 2003;48(1): 47-54. - Response | 0 | 0 |
| 2572 | 1 | 13 | 2543 2004 JOURNAL OF HUMAN GENETICS 49(2):97-101 Nagao K; Fujii K; Yamada M; Miyashita T Identification of a novel polymorphism involving a CGG repeat in the PTCH gene and a genome-wide screening of CGG-containing genes | 0 | 0 |
| 2573 | 0 | 0 | 2544 2004 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 48:287-287 Brown W; Nolin S; Dobkin C; Houck G; Glicksman A; et al. Frequency of fragile X in multiplex autism: Testing the AGRE families | 0 | 0 |
| 2574 | 0 | 0 | 2545 2004 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 48:288-288 Brown WT; Nolin S; Houck G; Ding X; Glicksman A; et al. The fragile X syndrome (FXS): Screening and prenatal diagnosis | 0 | 0 |
| 2575 | 0 | 0 | 2546 2004 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 48:294-294 Turk J; Das D; Howlin P; Barber N; Mottaleb M; et al. A follow-up of intellectual, social, communicatory & adaptive functioning in boys & young men with fragile X syndrome | 0 | 0 |
| 2576 | 0 | 0 | 2547 2004 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 48:294-294 Einfeld SL; Tonge BJ; Turner G; Smith E Longitudinal course of behavioural and emotional problems in Prader-Willi, Fragile X, Williams and Down syndromes | 0 | 0 |
| 2577 | 0 | 0 | 2548 2004 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 48:324-324 Abbeduto L; Murphy MM Language, communication, and the behavioural phenotype of Down syndrome (DS): Insights from fragile X syndrome (FXS) and typical development | 0 | 0 |
| 2578 | 0 | 0 | 2549 2004 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 48:325-325 Abbeduto L; Murphy MM; Giles N; Bruno L; Richmond EK; et al. Understanding language in context: Comparisons of Down syndrome (DS) with fragile X syndrome and typical development | 0 | 0 |
| 2579 | 0 | 0 | 2550 2004 JOURNAL OF INVESTIGATIVE MEDICINE 52(1):S101-S101 Nowicki ST; Jacquemont S; Li L; Nguyen DV; Gregg JP; et al. An approach to identify epistatic genes involved in the development of autism spectrum disorder in patients with fragile X syndrome | 0 | 0 |
| 2580 | 0 | 0 | 2551 2004 JOURNAL OF MEDICAL GENETICS 41:S64-S64 Turner A; Myring J; Stephens M; Antoniadi T; Butler R The Problem with Premutations: Assessment of new methods for fragile-X screening. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2581 | 0 | 0 | 2552 2004 JOURNAL OF MEDICAL GENETICS 41:S82-S82 McConachie M; Conlin L; McKay F; Gillespie K; Berg J A false negative PCR result in a boy with Fragile X syndrome | 0 | 0 |
| 2582 | 10 | 16 | 2553 2004 JOURNAL OF MEDICAL GENETICS 41(4) Zhou Y; Law HY; Boehm CD; Yoon CS; Cutting GR; et al. Robust fragile X (CGG)(n) genotype classification using a methylation specific triple PCR assay | 0 | 0 |
| 2583 | 41 | 65 | 2555 2004 JOURNAL OF MOLECULAR BIOLOGY 343(1):43-53 Menon RP; Gibson TJ; Pastore A The C terminus of fragile X mental retardation protein interacts with the multi-domain ran-binding protein in the microtubule-organising centre | 0 | 0 |
| 2584 | 0 | 0 | 2556 2004 JOURNAL OF MOLECULAR DIAGNOSTICS 6(4):409-409 Lee JY; Zhang YT; Hopcus-Niccum D; Mulvihill JJ; Li SB A mosaicism of 45,X/46,XX/47,XXX uncovered by molecular fragile X testing | 0 | 0 |
| 2585 | 0 | 0 | 2557 2004 JOURNAL OF MOLECULAR DIAGNOSTICS 6(4):409-409 Williams J; Lyon E; Miller C; Mao R Chromosome aneuploidy detected by fragile X southern blot and PCR analysis | 0 | 0 |
| 2586 | 19 | 34 | 2558 2004 JOURNAL OF MOLECULAR HISTOLOGY 35(4):389-395 Reis SA; Willemsen R; van Unen L; Hoogeveen AT; Oostra BA Prospects of TAT-mediated protein therapy for fragile X syndrome | 0 | 0 |
| 2587 | 1 | 1 | 2563 2004 JOURNAL OF NEUROSCIENCE 24(50):CP3-CP4 Gabel LA; Won S; Kawai H; McKinney M; Tartakoff AM; et al. Visual experience regulates transient expression and dendritic localization of fragile X mental retardation protein (vol 24, pg 10579, 2004) | 0 | 0 |
| 2588 | 7 | 21 | 2564 2004 JOURNAL OF THE NEUROLOGICAL SCIENCES 227(1):115-118 Garland EM; Vnencak-Jones CL; Biaggioni I; Davis TL; Montine TJ; et al. Fragile X gene premutation in multiple system atrophy | 0 | 0 |
| 2589 | 0 | 0 | 2565 2004 LANCET NEUROLOGY 3(12):701-701 Nelson R Drosophila model increases understanding of fragile-X syndrome | 0 | 0 |
| 2590 | 0 | 0 | 2566 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):1-2 Crnic LS; Hagerman R Preface: Fragile X syndrome: Frontiers of understanding gene-brain-behavior relationships | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2591 | 15 | 45 | 2572 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):42-48 Berry-Kravis E; Potanos K Psychopharmacology in fragile X syndrome - Present and future | 0 | 0 |
| 2592 | 7 | 66 | 2577 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):75-81 Rattazzi MC; LaFauci G; Brown WT Prospects for gene therapy in the fragile X syndrome | 0 | 0 |
| 2593 | 15 | 36 | 2578 2004 MOLECULAR BRAIN RESEARCH 131(1-2):101-109 Lauterborn JC Stress induced changes in cortical and hypothalamic c-fos expression are altered in fragile X mutant mice | 0 | 0 |
| 2594 | 1 | 50 | 2580 2004 MOLECULAR MICROBIOLOGY 54(3):742-754 Blaha B; Semsey S; Ferenczi S; Csiszovszki Z; Papp PP; et al. A proline tRNA(CGG) gene encompassing the attachment site of temperate phage 16-3 is functional and convertible to suppressor tRNA | 0 | 0 |
| 2595 | 0 | 0 | 2582 2004 MOVEMENT DISORDERS 19:S20-S20 Zhao Y; Puong K; Law H; Wong M; Ng I; et al. Fragile X premutation alleles in patients with sporadic cerebellar ataxia | 0 | 0 |
| 2596 | 0 | 0 | 2583 2004 MOVEMENT DISORDERS 19:S21-S21 Hall DA; Pelak VS; Hagerman RJ; Hagerman PJ; Leehey MA Ocular motility in Fragile X premutation carriers and Fragile X associated tremor/ataxia syndrome (FXTAS) | 0 | 0 |
| 2597 | 0 | 0 | 2584 2004 MOVEMENT DISORDERS 19:S338-S338 Leehey MA; Berry-Kravis E; Jacquemont S; Zhang L; Hagerman R; et al. Misdiagnosis of fragile X associated tremor/ataxia syndrome (FXTAS) | 0 | 0 |
| 2598 | 0 | 0 | 2585 2004 MOVEMENT DISORDERS 19:S339-S339 Leehey MA; Zhang L; Wheelock V; Tassone F; Hagerman R; et al. A preliminary observation: Increased frequency of fragile X expanded alleles in patients that meet diagnostic criteria for MSA | 0 | 0 |
| 2599 | 0 | 0 | 2586 2004 MOVEMENT DISORDERS 19:S359-S360 Di Maria E; Grasso M; Abbruzzese G; Mandich P; Ratto S; et al. The role for Fragile X premutation in essential tremor and spinocerebellar ataxia: Findings from two cohorts of Italian patients | 0 | 0 |
| 2600 | 0 | 0 | 2587 2004 MOVEMENT DISORDERS 19:S444-S444 Puong K; Zhao Y; Law H; Wong M; Ng I; et al. Screening for Fragile X premutation alleles in patients with essential tremor | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2601 | 0 | 0 | 2588 2004 MOVEMENT DISORDERS 19(9):1122-1122 Leehey MA; Hall D; Rice C; Jacquemont S; Zhang L; et al. The clinical course of fragile X-associated tremor/ataxia syndrome (FXTAS). | 0 | 0 |
| 2602 | 0 | 0 | 2589 2004 MOVEMENT DISORDERS 19(9):1127-1127 Hall DA; Rice CD; Hagerman RR; Hagerman PR; Berry-Kravis E; et al. Medical treatment for the fragile x-associated tremor/ataxia syndrome. | 0 | 0 |
| 2603 | 1 | 2 | 2592 2004 NATURE REVIEWS NEUROSCIENCE 5(1):4-4 Jones R Neurological disorders: Fragile X functions | 0 | 0 |
| 2604 | 0 | 0 | 2593 2004 NEUROBIOLOGY OF AGING 25:S434-S434 Westmark CJ; Malter JS FMRP mediates mGluR1-activated translation of APP | 0 | 0 |
| 2605 | 0 | 0 | 2594 2004 NEUROLOGY 62(7):A48-A48 Hagerman PJ; Jacquemont S; Hagerman RJ; Leehey MA; Hall DA; 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 |
| 2606 | 8 | 37 | 2596 2004 NEUROLOGY 63(9):1634-1639 Kogan CS; Bertone A; Cornish K; Boutet I; Kaloustian VMD; et al. Integrative cortical dysfunction and pervasive motion perception deficit in fragile X syndrome | 0 | 0 |
| 2607 | 5 | 7 | 2597 2004 NEUROLOGY 63(11):2188-2189 Pugliese P; Annesi G; Cutuli N; Arabia G; Nicoletti G; et al. The fragile X premutation presenting as postprandial hypotension | 0 | 0 |
| 2608 | 51 | 75 | 2598 2004 NEUROLOGY INDIA 52(1):36-42 Pandey UB; Phadke SR; Mittal B Molecular diagnosis and genetic counseling for fragile X mental retardation | 0 | 0 |
| 2609 | 52 | 101 | 2599 2004 NEUROPSYCHOLOGIA 42(14):1934-1947 Moore CJ; Daly EM; Schmitz N; Tassone F; Tysoe C; et al. A neuropsychological investigation of male premutation carriers of fragile X syndrome | 0 | 0 |
| 2610 | 6 | 23 | 2600 2004 NEUROREPORT 15(10):1579-1583 Greicius MD; Boyett-Anderson JM; Menon V; Reiss AL Reduced basal forebrain and hippocampal activation during memory encoding in girls with fragile X syndrome | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2611 | 24 | 42 | 2601 2004 NEUROREPORT 15(16):2447-2450 Veneri M; Zalfa F; Bagni C FMRP and its target RNAs: fishing for the specificity | 0 | 0 |
| 2612 | 18 | 44 | 2604 2004 NUCLEIC ACIDS RESEARCH 32(14):4145-4154 Khateb S; Weisman-Shomer P; Hershco I; Loeb LA; Fry M Destabilization of tetraplex structures of the fragile X repeat sequence (CGG)(n) is mediated by homolog-conserved domains in three members of the hnRNP family | 0 | 0 |
| 2613 | 0 | 1 | 2605 2004 PRAXIS DER KINDERPSYCHOLOGIE UND KINDERPSYCHIATRIE 53(8):593-594 Irblich D The fragile X syndrome - A guide for parents | 0 | 0 |
| 2614 | 6 | 8 | 2606 2004 PRENATAL DIAGNOSIS 24(1):67-68 Delatycki MB; Sheffield LJ; Wake S; Cohen J Screening approach for Fragile X syndrome | 0 | 0 |
| 2615 | 0 | 1 | 2607 2004 PRENATAL DIAGNOSIS 24(1):68-69 Wald NJ; Morris JK Reply: Prenatal screen for Fragile X syndrome | 0 | 0 |
| 2616 | 6 | 12 | 2608 2004 PRIMARY CARE 31(3):621-+ Wiesner GL; Cassidy SB; Grimes SJ; Matthews AL; Acheson LS Clinical consult: developmental delay/fragile X syndrome | 0 | 0 |
| 2617 | 14 | 57 | 2609 2004 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 101(10):3615-3620 Menon V; Leroux J; White CD; Reiss AL Frontostriatal deficits in fragile X syndrome: Relation to FMR1 gene expression | 0 | 0 |
| 2618 | 15 | 21 | 2612 2004 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 101(50):17329-17330 Miyashiro K; Eberwine J Fragile X syndrome: (What's) lost in translation? | 0 | 0 |
| 2619 | 28 | 50 | 2614 2004 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 101(50):17504-17509 Weiler IJ; Spangler CC; Klintsova AY; Grossman AW; Kim SH; et al. Fragile X mental retardation protein is necessary for neurotransmitter-activated protein translation at synapses | 0 | 0 |
| 2620 | 1 | 1 | 2615 2004 PROTEIN EXPRESSION AND PURIFICATION 37(1):264-264 McNulty DE; Claffee BA; Huddleston MJ; Kane JF Mistranslational errors associated with the rare arginine codon CGG in Escherichia coli (vol 27, pg 365, 2003) | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2621 | 3 | 53 | 2616 2004 QUALITATIVE HEALTH RESEARCH 14(6):741-759 Medved MI; Brockmeier J Making sense of traumatic experiences: Telling your life with fragile X syndrome | 0 | 0 |
| 2622 | 0 | 1 | 2617 2004 REPRODUCTIVE BIOMEDICINE ONLINE 8(3):337-337 [Anon] Late onset fragile X syndrome | 0 | 0 |
| 2623 | 2 | 7 | 2618 2004 REVISTA DE NEUROLOGIA 38(1):7-11 Artigas-Pallares J; Brun-Gasca C Can the behavioural phenotype of Fragile X syndrome be attributed to mental retardation and to attention deficit hyperactivity disorder? | 0 | 0 |
| 2624 | 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 |
| 2625 | 28 | 50 | 2621 2005 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 132A(1):25-32 Skinner M; Hooper S; Hatton DD; Robert J; Mirrett P; et al. Mapping nonverbal IQ in young boys with fragile X syndrome | 0 | 0 |
| 2626 | 12 | 18 | 2622 2005 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 132A(2):210-214 Angeli CB; Capelli LP; Auricchio MTBM; Vianna-Morgante AM; Mingroni-Netto RC; et al. AGG interspersion patterns in the CGG repeat of the FMR1 gene and linked DXS548/FRAXAC1 haplotypes in Brazilian populations | 0 | 0 |
| 2627 | 5 | 13 | 2625 2005 ARCHIVES DE PEDIATRIE 12(2):176-179 Vantalon V; Briard-Luginbuhl V; Mouren MC Fragile X syndrome and very early onset schizophrenia: a female case study | 0 | 0 |
| 2628 | 10 | 47 | 2626 2005 BIOCHEMICAL JOURNAL 386:297-303 Kumari D; Gabrielian A; Wheeler D; Usdin K The roles of Sp1, Sp3, USF1/USF2 and NRF-1 in the regulation and three-dimensional structure of the Fragile X mental retardation gene promoter | 0 | 0 |
| 2629 | 29 | 49 | 2627 2005 BRAIN AND COGNITION 57(1):53-60 Cornish K; Kogan C; Turk J; Manly T; James N; et al. The emerging fragile X premutation phenotype: Evidence from the domain of social cognition | 0 | 0 |
| 2630 | 17 | 20 | 2628 2005 CELLULAR AND MOLECULAR LIFE SCIENCES 62(2):251-252 Zalfa F; Bagni C Another view of the role of FMRP in translational regulation | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2631 | 16 | 52 | 2629 2005 DEVELOPMENTAL CELL 8(1):43-52 Zarnescu DC; Jin P; Betschinger J; Nakamoto M; Wang Y; et al. Fragile X protein functions with Lgl and the PAR complex in flies and mice | 0 | 0 |
| 2632 | 9 | 43 | 2630 2005 DEVELOPMENTAL CELL 8(3):331-342 Costa A; Wang Y; Dockendorff TC; Erdjument-Bromage H; Tempst P; et al. The Drosophila fragile X protein functions as a negative regulator in the orb autoregulatory pathway | 0 | 0 |
| 2633 | 1 | 33 | 2631 2005 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 47(2):94-104 Weiskop S; Richdale A; Matthews J Behavioural treatment to reduce sleep problems in children with autism or fragile X syndrome | 0 | 0 |
| 2634 | 0 | 1 | 2632 2005 EDUCATIONAL REVIEW 57(2):258-260 Reid G Educating children with Fragile X syndrome | 0 | 0 |
| 2635 | 19 | 26 | 2633 2005 FEBS JOURNAL 272(3):872-878 Pozdnyakova I; Regan L New insights into Fragile X syndrome - Relating genotype to phenotype at the molecular level | 0 | 0 |
| 2636 | 23 | 68 | 2634 2005 HUMAN MOLECULAR GENETICS 14(6):835-844 Castets M; Schaeffer C; Bechara E; Schenck A; Khandjian EW; et al. FMRP interferes with the Rac1 pathway and controls actin cytoskeleton dynamics in murine fibroblasts | 0 | 0 |
| 2637 | 2 | 4 | 2635 2005 JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION 293(3):296-296 Toft M; Farrer M Premutation alleles and fragile X-associated tremor/ataxia syndrome | 0 | 0 |
| 2638 | 1 | 3 | 2636 2005 JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION 293(3):296-297 Deng H; Le WD; Jankovic J Premutation alleles and fragile X-associated tremor/ataxia syndrome - Reply | 0 | 0 |
| 2639 | 21 | 46 | 2637 2005 JOURNAL OF BIOLOGICAL CHEMISTRY 280(6):4498-4503 Mulvihill DJ; Edamura KN; Hagerman KA; Pearson CE; Wang YH Effect of CAT or AGG interruptions and CpG methylation on nucleosome assembly upon trinucleotide repeats on spinocerebellar ataxia, type 1 and fragile X syndrome | 0 | 0 |
| 2640 | 23 | 47 | 2638 2005 JOURNAL OF BIOLOGICAL CHEMISTRY 280(7):5750-5763 Garnon J; Lachance C; Di Marco S; Hel Z; Marion D; et al. Fragile X-related protein FXR1P regulates proinflammatory cytokine tumor necrosis factor expression at the post-transcriptional level | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2641 | 3 | 8 | 2639 2005 JOURNAL OF CLINICAL NEUROSCIENCE 12(1):42-43 Storey E; Billimoria P Increased T-2 signal in the middle cerebellar peduncles on MRI is not specific for fragile X premutation syndrome | 0 | 0 |
| 2642 | 0 | 0 | 2640 2005 JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY 76(1):151-151 Ealing J; Mavrogiannis LA; Kingston H; Cockburn DJ; Taylor GR; et al. An atypical tetra nucleotide expansion in DM2 (PROMM) | 0 | 0 |
| 2643 | 25 | 61 | 2641 2005 MOLECULAR & CELLULAR PROTEOMICS 4(3):278-290 Zhang YQ; Friedman DB; Wang Z; Woodruff E; Pan LY; et al. Protein expression profiling of the Drosophila fragile X mutant brain reveals up-regulation of monoamine synthesis | 0 | 0 |
| 2644 | 4 | 10 | 2642 2005 NEURON 45(5):642-644 Dolen G; Bear MF Courting a cure for Fragile X | 0 | 0 |
| 2645 | 19 | 34 | 2644 2005 NEUROSCIENCE LETTERS 377(3):141-146 El Idrissi A; Ding XH; Scalia J; Trenkner E; Brown WT; et al. Decreased GABA(A) receptor expression in the seizure-prone fragile X mouse | 0 | 0 |
| 2646 | 24 | 45 | 2645 2005 NUCLEIC ACIDS RESEARCH 33(2):451-463 Napierala M; Michalowski D; de Mezer M; Krzyzosiak WJ Facile FMR1 mRNA structure regulation by interruptions in CGG repeats | 0 | 0 |
| 2647 | 29 | 46 | 2646 2005 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 102(6):2180-2185 Aschrafi A; Cunningham BA; Edelman GM; Vanderklish PW The fragile X mental retardation protein and group I metabotropic glutamate receptors regulate levels of mRNA granules in brain | 0 | 0 |