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5. Localisation of the Becker muscular dystrophy gene on the short arm of the X chromosome by linkage to cloned DNA sequences. Kingston HM; Sarfarazi M; Thomas NS; Harper PS Hum Genet; 1984; 67(1):6-17. PubMed ID: 6086495 [TBL] [Abstract][Full Text] [Related]
6. Possibilities and problems in genomic diagnosis of Duchenne muscular dystrophy with molecular probes. Speer A; Davies K; McGlade S; Hanke R; Spiegler AW; Szibor R; Sommer D; Herrmann F; Coutelle C Biomed Biochim Acta; 1986; 45(7):K19-27. PubMed ID: 2878658 [TBL] [Abstract][Full Text] [Related]
7. Carrier detection and gene analysis of Duchenne muscular dystrophy. Pearson PL; van Ommen GJ; Bakker E Cold Spring Harb Symp Quant Biol; 1986; 51 Pt 1():353-8. PubMed ID: 2884063 [No Abstract] [Full Text] [Related]
8. Isolation of the gene for Duchenne muscular dystrophy. Singh DN Indian J Pediatr; 1988; 55(2):177-82. PubMed ID: 2900215 [No Abstract] [Full Text] [Related]
9. [Uses of RFLP analysis in detecting Duchenne muscular dystrophy gene carrier]. Chen F Zhonghua Yi Xue Za Zhi; 1991 Jun; 71(6):339-41. PubMed ID: 1687519 [No Abstract] [Full Text] [Related]
12. DNA probes for carrier identification in Duchenne muscular dystrophy. Worton RG Clin Chem; 1989 Apr; 35(4):519-20. PubMed ID: 2564816 [No Abstract] [Full Text] [Related]
13. Evidence supporting tight linkage of X-linked Emery-Dreifuss muscular dystrophy to the factor VIII:C gene. Wehnert M; Machill G; Grimm T; Janka M; Camman R; Schröder W; Herrmann FH Hum Hered; 1991; 41(6):364-9. PubMed ID: 1686773 [TBL] [Abstract][Full Text] [Related]
14. 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]
15. MspI RFLP for Duchenne muscular dystrophy cDNA subclone 9. Wagner M; Reiss J; Hentemann M; Thies U Nucleic Acids Res; 1989 Apr; 17(8):3328. PubMed ID: 2471152 [No Abstract] [Full Text] [Related]
16. Carrier status diagnosis in Duchenne muscular dystrophy with "conformational" DNA polymorphism. Zietkiewicz E; Simard LR; Melançon SB; Vanasse M; Labuda D Lancet; 1992 Jan; 339(8785):134. PubMed ID: 1345868 [No Abstract] [Full Text] [Related]
17. Evidence for a sperm mutation resulting in Duchenne muscular dystrophy. Børresen AL; Heiberg A; Møller P; Berg K Clin Genet; 1987 Sep; 32(3):187-91. PubMed ID: 2887319 [TBL] [Abstract][Full Text] [Related]
18. [Carrier detection and gene analysis in a Duchenne muscular dystrophy family]. Lu FM Zhonghua Shen Jing Jing Shen Ke Za Zhi; 1990 Aug; 23(4):231-3, 255. PubMed ID: 1979269 [TBL] [Abstract][Full Text] [Related]
19. 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]
20. Dystrophin analysis in the diagnosis of muscular dystrophy. Norman AM; Hughes HE; Gardner-Medwin D; Nicholson LV Arch Dis Child; 1989 Oct; 64(10):1501-3. PubMed ID: 2684033 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]