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2. X-linked mental retardation: caveats in genetic counselling. Partington MW Am J Med Genet; 1986; 23(1-2):101-9. PubMed ID: 3953640 [No Abstract] [Full Text] [Related]
3. Seventh International Workshop on the Fragile X and X-linked Mental Retardation. Tranebjaerg L; Lubs HA; Borghgraef M; Brown WT; Fisch G; Fryns JP; Hagerman R; Jacobs PA; Mandel JL; Mulley J; Oostra B; Schwartz C; Sherman S; Willard H; Willems P Am J Med Genet; 1996 Jul; 64(1):1-14. PubMed ID: 8826442 [No Abstract] [Full Text] [Related]
4. Some problems in the genetics of X-linked mental retardation. Tariverdian G; Vogel F Cytogenet Cell Genet; 2000; 91(1-4):278-84. PubMed ID: 11173869 [TBL] [Abstract][Full Text] [Related]
5. Population based prenatal screening for the fragile X syndrome. Palomaki GE J Med Screen; 1994 Jan; 1(1):65-72. PubMed ID: 8790488 [No Abstract] [Full Text] [Related]
6. Fragile X syndrome: a major cause of X-linked mental retardation. Butler MG Compr Ther; 1988 Jul; 14(7):3-7. PubMed ID: 3060303 [No Abstract] [Full Text] [Related]
7. The recurrence risks for mild idiopathic mental retardation. Bundey S; Thake A; Todd J J Med Genet; 1989 Apr; 26(4):260-6. PubMed ID: 2785601 [TBL] [Abstract][Full Text] [Related]
8. The fragile-X syndrome. On the way to a behavioural phenotype. Turk J Br J Psychiatry; 1992 Jan; 160():24-35. PubMed ID: 1544010 [TBL] [Abstract][Full Text] [Related]
9. The FMR2 gene, FRAXE and non-specific X-linked mental retardation: clinical and molecular aspects. Gecz J Ann Hum Genet; 2000 Mar; 64(Pt 2):95-106. PubMed ID: 11246464 [TBL] [Abstract][Full Text] [Related]
10. 9th international workshop on fragile X syndrome and X-linked mental retardation. Fryns JP; Borghgraef M; Brown TW; Chelly J; Fisch GS; Hamel B; Hanauer A; Lacombe D; Luo L; MacPherson JN; Mandel JL; Moraine C; Mulley J; Nelson D; Oostra B; Partington M; Ramakers GJ; Ropers HH; Rousseau F; Schwartz C; Steinbach P; Stoll C; Tranebjaerg L; Turner G; Van Bokhoven H; Vianna-Morgante A Am J Med Genet; 2000 Oct; 94(5):345-60. PubMed ID: 11050616 [No Abstract] [Full Text] [Related]
11. Recurrence risks in undiagnosed mental retardation. Turner G; Partington M J Med Genet; 2000 Dec; 37(12):E45. PubMed ID: 11106363 [No Abstract] [Full Text] [Related]
12. Syndromal mental retardation due to mutations in a regulator of gene expression. Gibbons RJ; Picketts DJ; Higgs DR Hum Mol Genet; 1995; 4 Spec No():1705-9. PubMed ID: 8541868 [TBL] [Abstract][Full Text] [Related]
13. Conference report: Fourth International Workshop on the fragile X and X-linked mental retardation. Brown WT; Jenkins E; Neri G; Lubs H; Shapiro LR; Davies KE; Sherman S; Hagerman R; Laird C Am J Med Genet; 1991; 38(2-3):158-72. PubMed ID: 1673296 [No Abstract] [Full Text] [Related]
14. A community study of severe mental retardation in the West Midlands and the importance of the fragile X chromosome in its aetiology. Bundey S; Webb TP; Thake A; Todd J J Med Genet; 1985 Aug; 22(4):258-66. PubMed ID: 4045951 [TBL] [Abstract][Full Text] [Related]
15. Evidence that a dodecamer duplication in the gene HOPA in Xq13 is not associated with mental retardation. Friez MJ; Essop FB; Krause A; Castiglia L; Ragusa A; Sossey-Alaoui K; Nelson RL; May MM; Michaelis RC; Srivastava AK; Schwartz CE; Stevenson RE; Goldman A; Villard L; Longshore JW Hum Genet; 2000 Jan; 106(1):36-9. PubMed ID: 10982179 [TBL] [Abstract][Full Text] [Related]
16. Fragile X chromosome related to mental retardation in males. McBride G JAMA; 1979 Oct; 242(17):1829-30. PubMed ID: 480609 [No Abstract] [Full Text] [Related]
17. X-linked mental retardation. Conference report: Fourth International Workshop on the fragile X and X-linked mental retardation. Am J Med Genet; 1991; 38(2-3):153. PubMed ID: 1673295 [No Abstract] [Full Text] [Related]
18. Fragile X syndrome: an important preventable cause of mental handicap. Kinnell HG Br Med J (Clin Res Ed); 1987 Sep; 295(6598):564-5. PubMed ID: 3117231 [No Abstract] [Full Text] [Related]
19. Moderate and mild mental retardation in the Martin-Bell syndrome. Webb T; Thake A J Ment Defic Res; 1991 Dec; 35 ( Pt 6)():521-8. PubMed ID: 1800751 [TBL] [Abstract][Full Text] [Related]