240 related articles for article (PubMed ID: 8552426)
1. 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]
2. A fragile gene.
Oostra BA; Willems PJ
Bioessays; 1995 Nov; 17(11):941-7. PubMed ID: 8526888
[TBL] [Abstract][Full Text] [Related]
3. Fragile X mental retardation syndrome: from pathogenesis to diagnostic issues.
Mandel JL; Biancalana V
Growth Horm IGF Res; 2004 Jun; 14 Suppl A():S158-65. PubMed ID: 15135801
[TBL] [Abstract][Full Text] [Related]
4. A deletion of 1.6 Kb proximal to the CGG repeat of the FMR1 gene causes fragile X-like psychological features.
Wiegers AM; Curfs LM; Meijer H; Oostra B; Fryns JP
Genet Couns; 1994; 5(4):377-80. PubMed ID: 7888141
[TBL] [Abstract][Full Text] [Related]
5. Fragile X syndrome and deletions in FMR1: new case and review of the literature.
Hammond LS; Macias MM; Tarleton JC; Shashidhar Pai G
Am J Med Genet; 1997 Nov; 72(4):430-4. PubMed ID: 9375726
[TBL] [Abstract][Full Text] [Related]
6. Preimplantation diagnosis for fragile X syndrome based on the detection of the non-expanded paternal and maternal CGG.
Sermon K; Seneca S; Vanderfaeillie A; Lissens W; Joris H; Vandervorst M; Van Steirteghem A; Liebaers I
Prenat Diagn; 1999 Dec; 19(13):1223-30. PubMed ID: 10660959
[TBL] [Abstract][Full Text] [Related]
7. Molecular diagnosis and genetic counseling for fragile X mental retardation.
Pandey UB; Phadke SR; Mittal B
Neurol India; 2004 Mar; 52(1):36-42. PubMed ID: 15069237
[TBL] [Abstract][Full Text] [Related]
8. Fragile X syndrome without CCG amplification has an FMR1 deletion.
Gedeon AK; Baker E; Robinson H; Partington MW; Gross B; Manca A; Korn B; Poustka A; Yu S; Sutherland GR
Nat Genet; 1992 Aug; 1(5):341-4. PubMed ID: 1302032
[TBL] [Abstract][Full Text] [Related]
9. [Experimental therapy: reactivation of the FMR1 gene involved in fragile X syndrome].
Chiurazzi P; Neri G
Rev Neurol; 2001 Oct; 33 Suppl 1():S62-5. PubMed ID: 12447822
[TBL] [Abstract][Full Text] [Related]
10. Rare variants in the promoter of the fragile X syndrome gene (FMR1).
Milà M; Castellví-Bel S; Sánchez A; Barceló A; Badenas C; Mallolas J; Estivill X
Mol Cell Probes; 2000 Apr; 14(2):115-9. PubMed ID: 10799273
[TBL] [Abstract][Full Text] [Related]
11. [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]
12. Contribution of the FMR1 gene mutation to human intellectual dysfunction.
Reiss AL; Freund LS; Baumgardner TL; Abrams MT; Denckla MB
Nat Genet; 1995 Nov; 11(3):331-4. PubMed ID: 7581460
[TBL] [Abstract][Full Text] [Related]
13. Long uninterrupted CGG repeats within the first exon of the human FMR1 gene are not intrinsically unstable in transgenic mice.
Lavedan C; Grabczyk E; Usdin K; Nussbaum RL
Genomics; 1998 Jun; 50(2):229-40. PubMed ID: 9653650
[TBL] [Abstract][Full Text] [Related]
14. Fragile X founder effects and new mutations in Finland.
Zhong N; Kajanoja E; Smits B; Pietrofesa J; Curley D; Wang D; Ju W; Nolin S; Dobkin C; Ryynänen M; Brown WT
Am J Med Genet; 1996 Jul; 64(1):226-33. PubMed ID: 8826481
[TBL] [Abstract][Full Text] [Related]
15. Intragenic loss of function mutations demonstrate the primary role of FMR1 in fragile X syndrome.
Lugenbeel KA; Peier AM; Carson NL; Chudley AE; Nelson DL
Nat Genet; 1995 Aug; 10(4):483-5. PubMed ID: 7670500
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. A methylation PCR approach for detection of fragile X syndrome.
Panagopoulos I; Lassen C; Kristoffersson U; Aman P
Hum Mutat; 1999; 14(1):71-9. PubMed ID: 10447261
[TBL] [Abstract][Full Text] [Related]
19. Novel polymorphism in the FMR1 gene resulting in a "pseudodeletion" of FMR1 in a commonly used fragile X assay.
Daly TM; Rafii A; Martin RA; Zehnbauer BA
J Mol Diagn; 2000 Aug; 2(3):128-31. PubMed ID: 11229516
[TBL] [Abstract][Full Text] [Related]
20. The full mutation in the FMR-1 gene of male fragile X patients is absent in their sperm.
Reyniers E; Vits L; De Boulle K; Van Roy B; Van Velzen D; de Graaff E; Verkerk AJ; Jorens HZ; Darby JK; Oostra B
Nat Genet; 1993 Jun; 4(2):143-6. PubMed ID: 8348152
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]