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2. Duchenne muscular dystrophy: the gene and the protein. Love DR; Davies KE Mol Biol Med; 1989 Feb; 6(1):7-17. PubMed ID: 2666821 [No Abstract] [Full Text] [Related]
3. X-linked muscular dystrophies: studies through functional assay and DNA polymorphisms. Romeo G; Rocchi M; Roncuzzi L; Ferlini A; Nobile C; Rugolo M Adv Neurol; 1988; 48():31-6. PubMed ID: 2891257 [No Abstract] [Full Text] [Related]
4. Diagnosis of Duchenne and Becker muscular dystrophies by DNA polymorphism. Akita Y; Ohno S; Goto J; Nakano I; Takatsu M; Sugita H; Suzuki K Jinrui Idengaku Zasshi; 1987 Jun; 32(2):71-82. PubMed ID: 2893850 [No Abstract] [Full Text] [Related]
5. Direct method for prenatal diagnosis and carrier detection in Duchenne/Becker muscular dystrophy using the entire dystrophin cDNA. Darras BT; Koenig M; Kunkel LM; Francke U Am J Med Genet; 1988 Mar; 29(3):713-26. PubMed ID: 2897793 [TBL] [Abstract][Full Text] [Related]
6. Molecular analysis of human muscular dystrophies. Davies KE; Forrest S; Smith T; Kenwrick S; Ball S; Dorkins H; Patterson M Muscle Nerve; 1987; 10(3):191-9. PubMed ID: 2882417 [TBL] [Abstract][Full Text] [Related]
12. Towards a complete linkage map of the human X chromosome. Davies KE; Williamson R Horiz Biochem Biophys; 1986; 8():1-50. PubMed ID: 2875929 [TBL] [Abstract][Full Text] [Related]
13. Dystrophin immunocytochemistry in muscle culture: detection of a carrier of Duchenne muscular dystrophy. Miranda AF; Francke U; Bonilla E; Martucci G; Schmidt B; Salviati G; Rubin M Am J Med Genet; 1989 Feb; 32(2):268-73. PubMed ID: 2648829 [TBL] [Abstract][Full Text] [Related]
18. A BanI RFLP at a deletion hotspot in the human dystrophin gene. Read AP; Mountford R Nucleic Acids Res; 1990 Jan; 18(2):385. PubMed ID: 1970164 [No Abstract] [Full Text] [Related]
19. X-linked muscular dystrophy--phenotypic/genotypic correlation. Guard E; Roadley G; Watt A; Mueller RF N Z Med J; 1992 Aug; 105(939):319. PubMed ID: 1501822 [No Abstract] [Full Text] [Related]