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8. Nucleotide and corresponding amino acid sequence of human adult and fetal cDNA coding for portions of the Duchenne muscular dystrophy (DMD) gene. Rosenthal A; Speer A; Billwitz H; Cross GS; Forrest SM; Davies KE Biomed Biochim Acta; 1988; 47(2):K13-5. PubMed ID: 3178779 [No Abstract] [Full Text] [Related]
9. Duchenne and Becker muscular dystrophy mutations: analysis using 2.6 kb of muscle cDNA from the 5' end of the gene. Smith TJ; Forrest SM; Cross GS; Davies KE Nucleic Acids Res; 1987 Dec; 15(23):9761-9. PubMed ID: 3697082 [TBL] [Abstract][Full Text] [Related]
10. An isolated case of Duchenne muscular dystrophy (DMD) in a female with a deletion of DMD cDNA. Yoshioka M; Yamamoto Y; Furuyama J Clin Genet; 1990 Dec; 38(6):474-8. PubMed ID: 2289321 [TBL] [Abstract][Full Text] [Related]
11. Characterization and cell type distribution of a novel, major transcript of the Duchenne muscular dystrophy gene. Rapaport D; Lederfein D; den Dunnen JT; Grootscholten PM; Van Ommen GJ; Fuchs O; Nudel U; Yaffe D Differentiation; 1992 Apr; 49(3):187-93. PubMed ID: 1377655 [TBL] [Abstract][Full Text] [Related]
12. The use of field-inversion gel electrophoresis for deletion detection in Duchenne muscular dystrophy. Chen JD; Denton MJ; Morgan G; Pearn JH; Mackinlay AG Am J Hum Genet; 1988 May; 42(5):777-80. PubMed ID: 3358426 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. Isolation of a conserved sequence deleted in Duchenne muscular dystrophy patients. Smith TJ; Wilson L; Kenwrick SJ; Forrest SM; Speer A; Coutelle C; Davies KE Nucleic Acids Res; 1987 Mar; 15(5):2167-74. PubMed ID: 3562224 [TBL] [Abstract][Full Text] [Related]
15. Characterization of a 4.8kb transcript from the Duchenne muscular dystrophy locus expressed in Schwannoma cells. Blake DJ; Love DR; Tinsley J; Morris GE; Turley H; Gatter K; Dickson G; Edwards YH; Davies KE Hum Mol Genet; 1992 May; 1(2):103-9. PubMed ID: 1301145 [TBL] [Abstract][Full Text] [Related]
16. Apo-dystrophin-3: a 2.2kb transcript from the DMD locus encoding the dystrophin glycoprotein binding site. Tinsley JM; Blake DJ; Davies KE Hum Mol Genet; 1993 May; 2(5):521-4. PubMed ID: 8518789 [TBL] [Abstract][Full Text] [Related]
17. Molecular genetics of Duchenne and Becker muscular dystrophy: emphasis on improved diagnosis. Kunkel LM; Beggs AH; Hoffman EP Clin Chem; 1989 Jul; 35(7 Suppl):B21-4. PubMed ID: 2663232 [TBL] [Abstract][Full Text] [Related]
18. Localisation of the endpoints of deletions in the 5' region of the Duchenne gene using a sequence isolated by chromosome jumping. Kenwrick SJ; Smith TJ; England S; Collins F; Davies KE Nucleic Acids Res; 1988 Feb; 16(4):1305-17. PubMed ID: 3347492 [TBL] [Abstract][Full Text] [Related]