204 related articles for article (PubMed ID: 9146995)
1. Fragile X syndrome.
Chakrabarti L; Davies KE
Curr Opin Neurol; 1997 Apr; 10(2):142-7. PubMed ID: 9146995
[TBL] [Abstract][Full Text] [Related]
2. Distribution of CGG repeat sizes within the fragile X mental retardation 1 (FMR1) homologue in a non-human primate population.
Garcia Arocena D; Breece KE; Hagerman PJ
Hum Genet; 2003 Oct; 113(5):371-6. PubMed ID: 12905066
[TBL] [Abstract][Full Text] [Related]
3. Fragile X syndrome (review).
Pimentel MM
Int J Mol Med; 1999 Jun; 3(6):639-45. PubMed ID: 10341296
[TBL] [Abstract][Full Text] [Related]
4. The fragile X syndrome.
de Vries BB; Halley DJ; Oostra BA; Niermeijer MF
J Med Genet; 1998 Jul; 35(7):579-89. PubMed ID: 9678703
[TBL] [Abstract][Full Text] [Related]
5. The effect of pre-mutation of X chromosome CGG trinucleotide repeats on brain anatomy.
Moore CJ; Daly EM; Tassone F; Tysoe C; Schmitz N; Ng V; Chitnis X; McGuire P; Suckling J; Davies KE; Hagerman RJ; Hagerman PJ; Murphy KC; Murphy DG
Brain; 2004 Dec; 127(Pt 12):2672-81. PubMed ID: 15483045
[TBL] [Abstract][Full Text] [Related]
6. Deletion of all CGG repeats plus flanking sequences in FMR1 does not abolish gene expression.
Grønskov K; Hjalgrim H; Bjerager MO; Brøndum-Nielsen K
Am J Hum Genet; 1997 Oct; 61(4):961-7. PubMed ID: 9382110
[TBL] [Abstract][Full Text] [Related]
7. Normal phenotype in two brothers with a full FMR1 mutation.
Smeets HJ; Smits AP; Verheij CE; Theelen JP; Willemsen R; van de Burgt I; Hoogeveen AT; Oosterwijk JC; Oostra BA
Hum Mol Genet; 1995 Nov; 4(11):2103-8. PubMed ID: 8589687
[TBL] [Abstract][Full Text] [Related]
8. Methylation mosaicism of 5'-(CGG)(n)-3' repeats in fragile X, premutation and normal individuals.
Genç B; Müller-Hartmann H; Zeschnigk M; Deissler H; Schmitz B; Majewski F; von Gontard A; Doerfler W
Nucleic Acids Res; 2000 May; 28(10):2141-52. PubMed ID: 10773084
[TBL] [Abstract][Full Text] [Related]
9. [From gene to disease; fragile X-syndrome: hereditary mental retardation due to a developmental gene].
de Vries LB; Oostra BA
Ned Tijdschr Geneeskd; 2001 Mar; 145(10):474-6. PubMed ID: 11268909
[TBL] [Abstract][Full Text] [Related]
10. [Detection of FMR-1 gene expression by RT-PCR].
Zheng L; Fan Y; Huang T; Zhu N; Shen Y; Wu G
Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1995 Dec; 17(6):407-11. PubMed ID: 9208564
[TBL] [Abstract][Full Text] [Related]
11. Complex behavior of simple repeats: the fragile X syndrome.
Oostra BA; Halley DJ
Pediatr Res; 1995 Nov; 38(5):629-37. PubMed ID: 8552426
[TBL] [Abstract][Full Text] [Related]
12. Triplet repeat polymorphism & fragile X syndrome in the Indian context.
Baskaran S; Naseerullah MK; Manjunatha KR; Chetan GK; Arthi R; Rao GV; Girimaji SR; Srinath S; Sheshadri S; Devi RR; Brahmachari V
Indian J Med Res; 1998 Jan; 107():29-36. PubMed ID: 9529778
[TBL] [Abstract][Full Text] [Related]
13. Nucleosome assembly on methylated CGG triplet repeats in the fragile X mental retardation gene 1 promoter.
Godde JS; Kass SU; Hirst MC; Wolffe AP
J Biol Chem; 1996 Oct; 271(40):24325-8. PubMed ID: 8798682
[TBL] [Abstract][Full Text] [Related]
14. [Molecular pathogenesis of fragile X syndrome].
Sielska D; Milewski M; Bal J
Med Wieku Rozwoj; 2002; 6(4):295-308. PubMed ID: 12810982
[TBL] [Abstract][Full Text] [Related]
15. Deletion in the FMR1 gene in a fragile-X male.
Mannermaa A; Pulkkinen L; Kajanoja E; Ryynänen M; Saarikoski S
Am J Med Genet; 1996 Aug; 64(2):293-5. PubMed ID: 8844068
[TBL] [Abstract][Full Text] [Related]
16. Molecular-intelligence correlations in young fragile X males with a mild CGG repeat expansion in the FMR1 gene.
Steyaert J; Borghgraef M; Legius E; Fryns JP
Am J Med Genet; 1996 Aug; 64(2):274-7. PubMed ID: 8844064
[TBL] [Abstract][Full Text] [Related]
17. Instability of a (CGG)98 repeat in the Fmr1 promoter.
Bontekoe CJ; Bakker CE; Nieuwenhuizen IM; van der Linde H; Lans H; de Lange D; Hirst MC; Oostra BA
Hum Mol Genet; 2001 Aug; 10(16):1693-9. PubMed ID: 11487573
[TBL] [Abstract][Full Text] [Related]
18. Stability of the FMR1 CGG repeat in a Basque sample.
Arrieta I; Gil A; Nuñez T; Telez M; Martinez B; Criado B; Lostao C
Hum Biol; 1999 Feb; 71(1):55-68. PubMed ID: 9972098
[TBL] [Abstract][Full Text] [Related]
19. Re-examination of factors associated with expansion of CGG repeats using a single nucleotide polymorphism in FMR1.
Gunter C; Paradee W; Crawford DC; Meadows KA; Newman J; Kunst CB; Nelson DL; Schwartz C; Murray A; Macpherson JN; Sherman SL; Warren ST
Hum Mol Genet; 1998 Nov; 7(12):1935-46. PubMed ID: 9811938
[TBL] [Abstract][Full Text] [Related]
20. Screening for FMR1 and FMR2 mutations in 222 individuals from Spanish special schools: identification of a case of FRAXE-associated mental retardation.
Milà M; Sànchez A; Badenas C; Brun C; Jiménez D; Villa MP; Castellví-Bel S; Estivill X
Hum Genet; 1997 Oct; 100(5-6):503-7. PubMed ID: 9341861
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]