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26. The linkage between the genes for colour-blindness and haemophilia in man. By Julia Bell and J.B.S. Haldane, 1937. Bell J; Haldane JB Ann Hum Genet; 1986 Jan; 50(1):3-34. PubMed ID: 3322165 [No Abstract] [Full Text] [Related]
27. Molecular biology of Duchenne and Becker's muscular dystrophy: clinical applications. Gutmann DH; Fischbeck KH Ann Neurol; 1989 Aug; 26(2):189-94. PubMed ID: 2673003 [TBL] [Abstract][Full Text] [Related]
29. Letter: Mutation in Duchenne muscular dystrophy. Tyler FH; Skolnick M N Engl J Med; 1976 Jul; 295(5):283-4. PubMed ID: 934200 [No Abstract] [Full Text] [Related]
30. The rationale of genetic counseling. Murphy EA J Pediatr; 1968 Jan; 72(1):121-30. PubMed ID: 4229313 [No Abstract] [Full Text] [Related]
31. The use of linked DNA polymorphisms for genotype prediction in families with Duchenne muscular dystrophy. Harper PS; O'Brien T; Murray JM; Davies KE; Pearson P; Williamson R J Med Genet; 1983 Aug; 20(4):252-4. PubMed ID: 6684693 [TBL] [Abstract][Full Text] [Related]
32. The muscular dystrophies. Bushby KM Baillieres Clin Neurol; 1994 Aug; 3(2):407-30. PubMed ID: 7952855 [TBL] [Abstract][Full Text] [Related]
33. Linkage of Tunisian autosomal recessive Duchenne-like muscular dystrophy to the pericentromeric region of chromosome 13q. Ben Othmane K; Ben Hamida M; Pericak-Vance MA; Ben Hamida C; Blel S; Carter SC; Bowcock AM; Petruhkin K; Gilliam TC; Roses AD Nat Genet; 1992 Dec; 2(4):315-7. PubMed ID: 1303286 [TBL] [Abstract][Full Text] [Related]
34. Immunological identification of a high molecular weight protein as a candidate for the product of the Duchenne muscular dystrophy gene. Kao L; Krstenansky J; Mendell J; Rammohan KW; Gruenstein E Proc Natl Acad Sci U S A; 1988 Jun; 85(12):4491-5. PubMed ID: 3288996 [TBL] [Abstract][Full Text] [Related]
38. Localization of the region homologous to the Duchenne muscular dystrophy locus on the mouse X chromosome. Heilig R; Lemaire C; Mandel JL; Dandolo L; Amar L; Avner P Nature; 1987 Jul 9-15; 328(6126):168-70. PubMed ID: 3600794 [TBL] [Abstract][Full Text] [Related]
39. Detection of gene deletion in patients of Duchenne muscular dystrophy/Becker muscular dystrophy using polymerase chain reaction. Sinha S; Pradhan S; Mittal RD; Mittal B Indian J Med Res; 1992 Oct; 96():297-301. PubMed ID: 1459673 [TBL] [Abstract][Full Text] [Related]