These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
215 related articles for article (PubMed ID: 7079652)
1. [Mental retardation linked to the X chromosome]. Lambotte C Rev Med Liege; 1982 Feb; 37(4):130-9. PubMed ID: 7079652 [No Abstract] [Full Text] [Related]
2. Fragile X-linked mental retardation: the Martin-Bell syndrome. Richards BW; Sylvester PE; Brooker C J Ment Defic Res; 1981 Dec; 25 Pt 4():253-6. PubMed ID: 7328634 [TBL] [Abstract][Full Text] [Related]
3. A marker X chromosome associated with nonspecific male mental retardation. The first South African cases. Venter PA; Gericke GS; Dawson B; Op't Hof J S Afr Med J; 1981 Nov; 60(21):807-11. PubMed ID: 7302747 [TBL] [Abstract][Full Text] [Related]
5. X-linked mental retardation with the fragile X. A study of 15 families. Mattei JF; Mattei MG; Aumeras C; Auger M; Giraud F Hum Genet; 1981; 59(4):281-9. PubMed ID: 7333582 [TBL] [Abstract][Full Text] [Related]
6. X-linked mental retardation with a fragile site in Xq and an inversion of chromosome no. 9. Howard-Peebles PN Hum Hered; 1982; 32(2):139-41. PubMed ID: 7201453 [TBL] [Abstract][Full Text] [Related]
7. A cytogenetic study of mentally retarded school children in Taiwan with special reference to the fragile X chromosome. Li SY; Tsai CC; Chou MY; Lin JK Hum Genet; 1988 Aug; 79(4):292-6. PubMed ID: 2970423 [TBL] [Abstract][Full Text] [Related]
8. 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]
9. Fragile X syndrome: a unique mutation in man. Nussbaum RL; Ledbetter DH Annu Rev Genet; 1986; 20():109-45. PubMed ID: 3545058 [No Abstract] [Full Text] [Related]
10. Expression of the fragile site Xq27 in fibroblasts. I. Detection of fra(X)(q27) in fibroblast clones from males with X-linked mental retardation. Steinbach P; Barbi G; Baur S; Wiedenmann A Hum Genet; 1983; 63(4):404-5. PubMed ID: 6683244 [TBL] [Abstract][Full Text] [Related]
11. X linked mental retardation: a family with a separate syndrome? Thompson EM; Gordon A; Baraitser M J Med Genet; 1989 Jun; 26(6):373-8. PubMed ID: 2738899 [TBL] [Abstract][Full Text] [Related]
12. Marker X chromosomes in nonspecific male mental retardation. Venter PA; Gericke GS S Afr Med J; 1980 Jun; 57(26):1066. PubMed ID: 7190736 [No Abstract] [Full Text] [Related]
13. A recognizable syndrome of sex-linked mental retardation, large testes, and marker X chromosome. Hecht JT; Moore CM; Scott CI South Med J; 1981 Dec; 74(12):1493-6. PubMed ID: 6947439 [No Abstract] [Full Text] [Related]
14. X-linked mental retardation with macro-orchidism and marker X chromosomes. Howard-Peebles PN; Stoddard GR Hum Genet; 1979 Sep; 50(3):247-51. PubMed ID: 489008 [TBL] [Abstract][Full Text] [Related]
15. Mental retardation, megalotestes and a marker X chromosome. Fitzsimmons J; McLachlan JI; Fitzsimmons E; Cooke P Practitioner; 1982 Apr; 226(1366):735-41. PubMed ID: 6953399 [No Abstract] [Full Text] [Related]
16. Marker X syndrome in an oriental family with probable transmission by a normal male. Rhoads FA; Oglesby AC; Mayer M; Jacobs PA Am J Med Genet; 1982 Jun; 12(2):205-17. PubMed ID: 7102725 [TBL] [Abstract][Full Text] [Related]
18. Bibliography on X-linked mental retardation, the fragile X and related subjects IV (1988). Spano LM; Opitz JM Am J Med Genet; 1988; 30(1-2):31-60. PubMed ID: 3052063 [No Abstract] [Full Text] [Related]
19. Fragile site X chromosomes and X-linked mental retardation in severely retarded boys in a northern Swedish county. A prevalence study. Blomquist HK; Gustavson KH; Holmgren G; Nordenson I; Sweins A Clin Genet; 1982 Mar; 21(3):209-14. PubMed ID: 7201364 [No Abstract] [Full Text] [Related]
20. Linkage analysis of X-linked mental retardation with and without fragile-X using factor IX gene probe. Choo KH; George D; Filby G; Halliday JL; Leversha M; Webb G; Danks DM Lancet; 1984 Aug; 2(8398):349. PubMed ID: 6146889 [No Abstract] [Full Text] [Related] [Next] [New Search]