134 related articles for article (PubMed ID: 8750357)
1. Screening for CGG trinucleotide repeat expansion in the fragile X mental retardation 1 gene in schizophrenic patients.
Jönsson E; Björck E; Wahlström J; Gustavsson P; Sedvall G
Psychiatr Genet; 1995; 5(4):157-60. PubMed ID: 8750357
[TBL] [Abstract][Full Text] [Related]
2. Molecular analysis of the (CGG)n expansion in the FMR-1 gene in 59 Spanish fragile X syndrome families.
Milà M; Kruyer H; Glover G; Sánchez A; Carbonell P; Castellví-Bell S; Volpini V; Rossell J; Gabarrón J; López I
Hum Genet; 1994 Oct; 94(4):395-400. PubMed ID: 7927336
[TBL] [Abstract][Full Text] [Related]
3. A point mutation in the FMR-1 gene associated with fragile X mental retardation.
De Boulle K; Verkerk AJ; Reyniers E; Vits L; Hendrickx J; Van Roy B; Van den Bos F; de Graaff E; Oostra BA; Willems PJ
Nat Genet; 1993 Jan; 3(1):31-5. PubMed ID: 8490650
[TBL] [Abstract][Full Text] [Related]
4. Fragile X syndrome: discordant levels of CGG repeat mosaicism in two brothers.
Mueller OT; Hartsfield JK; Amar MJ; Gallardo LA; Kousseff BG
Am J Med Genet; 1995 Aug; 60(4):302-6. PubMed ID: 7485265
[TBL] [Abstract][Full Text] [Related]
5. Mental status and fragile X expression in relation to FMR-1 gene mutation.
de Vries BB; Wiegers AM; de Graaff E; Verkerk AJ; Van Hemel JO; Halley DJ; Fryns JP; Curfs LM; Niermeijer MF; Oostra BA
Eur J Hum Genet; 1993; 1(1):72-9. PubMed ID: 8069653
[TBL] [Abstract][Full Text] [Related]
6. Analysis of a CGG sequence at the FMR-1 locus in fragile X families and in the general population.
Snow K; Doud LK; Hagerman R; Pergolizzi RG; Erster SH; Thibodeau SN
Am J Hum Genet; 1993 Dec; 53(6):1217-28. PubMed ID: 7902673
[TBL] [Abstract][Full Text] [Related]
7. Molecular and cytogenetic investigations of the fragile X region including the Frax A and Frax E CGG trinucleotide repeat sequences in families multiplex for autism and related phenotypes.
Gurling HM; Bolton PF; Vincent J; Melmer G; Rutter M
Hum Hered; 1997; 47(5):254-62. PubMed ID: 9358013
[TBL] [Abstract][Full Text] [Related]
8. Apparent regression of the CGG repeat in FMR1 to an allele of normal size.
Vits L; De Boulle K; Reyniers E; Handig I; Darby JK; Oostra B; Willems PJ
Hum Genet; 1994 Nov; 94(5):523-6. PubMed ID: 7959688
[TBL] [Abstract][Full Text] [Related]
9. Fragile X syndrome and the (CGG)n mutation: two families with discordant MZ twins.
Kruyer H; Milà M; Glover G; Carbonell P; Ballesta F; Estivill X
Am J Hum Genet; 1994 Mar; 54(3):437-42. PubMed ID: 8116613
[TBL] [Abstract][Full Text] [Related]
10. FMR1 gene deletion/reversion: a pitfall of fragile X carrier testing.
Gasteiger M; Grasbon-Frodl E; Neitzel B; Kooy F; Holinski-Feder E
Genet Test; 2003; 7(4):303-8. PubMed ID: 15000806
[TBL] [Abstract][Full Text] [Related]
11. Molecular genetic analysis of mentally retarded males with features of the fragile-X syndrome.
Butler MG; Pratesi R; Vnencak-Jones CL
J Intellect Disabil Res; 1995 Dec; 39 ( Pt 6)(Pt 6):544-53. PubMed ID: 8746743
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Molecular predictors of cognitive involvement in female carriers of fragile X syndrome.
Taylor AK; Safanda JF; Fall MZ; Quince C; Lang KA; Hull CE; Carpenter I; Staley LW; Hagerman RJ
JAMA; 1994 Feb; 271(7):507-14. PubMed ID: 8301764
[TBL] [Abstract][Full Text] [Related]
14. A deletion of 1.6 kb proximal to the CGG repeat of the FMR1 gene causes the clinical phenotype of the fragile X syndrome.
Meijer H; de Graaff E; Merckx DM; Jongbloed RJ; de Die-Smulders CE; Engelen JJ; Fryns JP; Curfs PM; Oostra BA
Hum Mol Genet; 1994 Apr; 3(4):615-20. PubMed ID: 8069307
[TBL] [Abstract][Full Text] [Related]
15. Variation of the CGG repeat in FMR-1 gene in normal and fragile X Chinese subjects.
Chen TA; Lu XF; Che PK; Ho WK
Ann Clin Biochem; 1997 Sep; 34 ( Pt 5)():517-20. PubMed ID: 9293305
[TBL] [Abstract][Full Text] [Related]
16. Hotspot for deletions in the CGG repeat region of FMR1 in fragile X patients.
de Graaff E; Rouillard P; Willems PJ; Smits AP; Rousseau F; Oostra BA
Hum Mol Genet; 1995 Jan; 4(1):45-9. PubMed ID: 7711733
[TBL] [Abstract][Full Text] [Related]
17. Polymerase chain reaction analysis of fragile X mutations.
Erster SH; Brown WT; Goonewardena P; Dobkin CS; Jenkins EC; Pergolizzi RG
Hum Genet; 1992; 90(1-2):55-61. PubMed ID: 1427787
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Absence of the fragile X CGG trinucleotide repeat expansion in girls diagnosed with a pervasive developmental disorder.
Meyer GA; Blum NJ; Hitchcock W; Fortina P
J Pediatr; 1998 Sep; 133(3):363-5. PubMed ID: 9738717
[TBL] [Abstract][Full Text] [Related]
20. Linkage analysis of the fragile X gene FMR-1 and schizophrenia: no evidence for linkage but report of a family with schizophrenia and an unstable triplet repeat.
Ashworth A; Abusaad I; Walsh C; Nanko S; Murray RM; Asherson P; McGuffin P; Gill M; Owen MJ; Collier DA
Psychiatr Genet; 1996; 6(2):81-6. PubMed ID: 8840394
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
