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.
152 related articles for article (PubMed ID: 7011031)
1. X-linked mental retardation. Turner G; Opitz JM Am J Med Genet; 1980; 7(4):407-15. PubMed ID: 7011031 [No Abstract] [Full Text] [Related]
2. Significance of phenotypic and chromosomal abnormalities in X-linked mental retardation (Martin-Bell or Renpenning syndrome). Jennings M; Hall JG; Hoehn H Am J Med Genet; 1980; 7(4):417-32. PubMed ID: 6938131 [TBL] [Abstract][Full Text] [Related]
3. X-linked mental retardation and an X-chromosome marker. Gerald PS N Engl J Med; 1980 Sep; 303(12):696-7. PubMed ID: 6931287 [No Abstract] [Full Text] [Related]
4. Fragile X-linked mental retardation. Kaiser-McCaw B; Hecht F; Cadien JD; Moore BC Am J Med Genet; 1980; 7(4):503-5. PubMed ID: 7211959 [No Abstract] [Full Text] [Related]
5. Fragile sites in human chromosomes II: demonstration of the fragile site Xq27 in carriers of X-linked mental retardation. Howard-Peebles PN Am J Med Genet; 1980; 7(4):497-501. PubMed ID: 6938133 [TBL] [Abstract][Full Text] [Related]
6. Nonspecific X-linked mental retardation I: a review with information from 24 new families. Herbst DS Am J Med Genet; 1980; 7(4):443-60. PubMed ID: 7011032 [TBL] [Abstract][Full Text] [Related]
7. X-linked mental retardation with macro-orchidism and marker-X chromosomes. Martin RH; Lin CC; Mathies BJ; Lowry RB Am J Med Genet; 1980; 7(4):433-41. PubMed ID: 6938132 [TBL] [Abstract][Full Text] [Related]
8. X-linked mental retardation: a study of 7 families. Jacobs PA; Glover TW; Mayer M; Fox P; Gerrard JW; Dunn HG; Herbst DS Am J Med Genet; 1980; 7(4):471-89. PubMed ID: 7211957 [TBL] [Abstract][Full Text] [Related]
9. [The role of the marker X chromosome in the diagnosis of Martin-Bell syndrome (review of the literature)]. Bessudnova SS; Il'inskikh NN Zh Nevropatol Psikhiatr Im S S Korsakova; 1990; 90(3):128-32. PubMed ID: 2163154 [No Abstract] [Full Text] [Related]
10. [Fragile X chromosome and X-linked mental retardation (author's transl)]. Fonatsch C; Flatz SD Wien Klin Wochenschr; 1982 Apr; 94(8):217-9. PubMed ID: 7101956 [TBL] [Abstract][Full Text] [Related]
11. [Sex-linked recessive mental retardation without specific clinical manifestations]. Denisova LV; Bedel'baeva KA Zh Nevropatol Psikhiatr Im S S Korsakova; 1983; 83(3):92-7. PubMed ID: 6683054 [No Abstract] [Full Text] [Related]
12. The fragile X chromosome: current methods. Hecht F; Jacky PB; Sutherland GR Am J Med Genet; 1982 Apr; 11(4):489-95. PubMed ID: 6211983 [No Abstract] [Full Text] [Related]
13. +2.71 LOD score at zero recombination is not sufficient for establishing linkage between X-linked mental retardation and X-chromosome markers. Robledo R; Melis P; Siniscalco M; Marchi J; Laficara F; Rinaldi A; Rocchi M; Filippi G Am J Med Genet; 1996 Jul; 64(1):134-6. PubMed ID: 8928707 [No Abstract] [Full Text] [Related]
14. Genetic localisation of MRX27 to Xq24-26 defines another discrete gene for non-specific X-linked mental retardation. Gedeon AK; Glass IA; Connor JM; Mulley JC Am J Med Genet; 1996 Jul; 64(1):121-4. PubMed ID: 8826461 [TBL] [Abstract][Full Text] [Related]
15. Nonspecific X-linked mental retardation II: the frequency in British Columbia. Herbst DS; Miller JR Am J Med Genet; 1980; 7(4):461-9. PubMed ID: 7211956 [TBL] [Abstract][Full Text] [Related]
16. Further linkage evidence for localization of mutational sites for nonsyndromic types of X-linked mental retardation at the pericentromeric region. Robledo R; Melis P; Laficara F; Marchi J; Rinaldi A; Siniscalco M; Filippi G Am J Med Genet; 1996 Jul; 64(1):107-12. PubMed ID: 8826459 [TBL] [Abstract][Full Text] [Related]
17. [X-chromosome-linked mental deficiency and the chromosome marker fra(X)(q28)]. Simola KO; Kähkönen M; Leisti J Duodecim; 1982; 98(7):526-34. PubMed ID: 6953010 [No Abstract] [Full Text] [Related]
18. Localization of two X-linked mental retardation (XLMR) genes to Xp: MRX37 gene at Xp22.31-p22.32 and a putative MRX gene on Xp22.11-p22.2. Bar-David S; Lerer I; Sarfaty CK; Kohan ZG; Meiner V; Zlotogora J; Abeliovich D Am J Med Genet; 1996 Jul; 64(1):83-8. PubMed ID: 8826456 [TBL] [Abstract][Full Text] [Related]