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5. A branching non-linear autoregressive model for the transmission of the fragile X dynamic repeat mutation. Huggins RM; Loesch DZ; Sherman SL Ann Hum Genet; 1998 Jul; 62(Pt 4):337-47. PubMed ID: 9924611 [TBL] [Abstract][Full Text] [Related]
6. [Direct molecular analysis of FMR-1 gene mutation in patients with fragile Xq syndrome and their families]. Alliende MA; Urzúa B; Valiente A; Cortés F; Curotto B; Rojas C Rev Med Chil; 1998 Dec; 126(12):1435-46. PubMed ID: 10349157 [TBL] [Abstract][Full Text] [Related]
7. 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]
8. [Fragile X syndrome, a disease caused by defects in an RNA-binding protein]. Siomi MC; Siomi H Tanpakushitsu Kakusan Koso; 2003 Mar; 48(4 Suppl):480-6. PubMed ID: 12696157 [No Abstract] [Full Text] [Related]
9. Compound heterozygous female with fragile X syndrome. Linden MG; Tassone F; Gane LW; Hills JL; Hagerman RJ; Taylor AK Am J Med Genet; 1999 Apr; 83(4):318-21. PubMed ID: 10208169 [TBL] [Abstract][Full Text] [Related]
10. Reverse mutations in the fragile X syndrome. Brown WT; Houck GE; Ding X; Zhong N; Nolin S; Glicksman A; Dobkin C; Jenkins EC Am J Med Genet; 1996 Aug; 64(2):287-92. PubMed ID: 8844067 [TBL] [Abstract][Full Text] [Related]
11. In vivo footprinting analysis of the FMR1 gene: proposals concerning gene regulation in high-functioning males. Schwemmle S Am J Med Genet; 1999 May; 84(3):266-7. PubMed ID: 10331604 [No Abstract] [Full Text] [Related]
12. No apparent involvement of the FMR1 gene in five patients with phenotypic manifestations of the fragile X syndrome. Chiurazzi P; de Graaff E; Ng J; Verkerk AJ; Wolfson S; Fisch GS; Kozak L; Neri G; Oostra BA Am J Med Genet; 1994 Jul; 51(4):309-14. PubMed ID: 7942992 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. Characterization of the full fragile X syndrome mutation in fetal gametes. Malter HE; Iber JC; Willemsen R; de Graaff E; Tarleton JC; Leisti J; Warren ST; Oostra BA Nat Genet; 1997 Feb; 15(2):165-9. PubMed ID: 9020841 [TBL] [Abstract][Full Text] [Related]
16. [Diagnosis of Martin-Bell syndrome based on an analysis of the structural-functional changes in the 5'-untranslated region of the FMR1 gene]. Strel'nikov VV; Nemtsova MV; Chesnokova GG; Kuleshov NP; Zaletaev DV Mol Biol (Mosk); 1999; 33(2):330-6. PubMed ID: 10377581 [No Abstract] [Full Text] [Related]
17. Analysis of unstable DNA sequence in FMR1 gene in Polish families with fragile X syndrome. Milewski M; Zygulska M; Bal J; Deelen WH; Obersztyn E; Bocian E; Halley DJ; Horst J; Mazurczak T Acta Biochim Pol; 1996; 43(2):383-8. PubMed ID: 8862184 [TBL] [Abstract][Full Text] [Related]
18. 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]
19. Timing of the absence of FMR1 expression in full mutation chorionic villi. Willemsen R; Bontekoe CJ; Severijnen LA; Oostra BA Hum Genet; 2002 Jun; 110(6):601-5. PubMed ID: 12107447 [TBL] [Abstract][Full Text] [Related]
20. Fragile X syndrome and other dynamic mutation diseases. Sutherland GR; Richards RI Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():77-85. PubMed ID: 8629146 [No Abstract] [Full Text] [Related] [Next] [New Search]