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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

97 related articles for article (PubMed ID: 2876742)

  • 1. Isolating the gene for Duchenne muscular dystrophy.
    Harper PS
    Br Med J (Clin Res Ed); 1986 Sep; 293(6550):773-4. PubMed ID: 2876742
    [No Abstract]   [Full Text] [Related]  

  • 2. 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]  

  • 3. RFLP for HindIII at the Duchenne muscular dystrophy gene.
    Prior TW; Friedman KJ; Silverman LM
    Nucleic Acids Res; 1989 Mar; 17(6):2370. PubMed ID: 2565028
    [No Abstract]   [Full Text] [Related]  

  • 4. RFLP for Duchenne muscular dystrophy cDNA clone 30-2.
    Walker AP; Bartlett RJ; Laing NG; Siddique T; Yamaoka LH; Chen JC; Hung WY; Roses AD
    Nucleic Acids Res; 1988 Sep; 16(18):9072. PubMed ID: 2902573
    [No Abstract]   [Full Text] [Related]  

  • 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]  

  • 10. RFLP for Duchenne muscular dystrophy cDNA clone 44-1.
    Laing NG; Siddique T; Bartlett RJ; Yamaoka LH; Chen JC; Walker AP; Hung WY; Roses AD
    Nucleic Acids Res; 1988 Jul; 16(14B):7209. PubMed ID: 2900496
    [No Abstract]   [Full Text] [Related]  

  • 11. Gene mapping and the muscular dystrophies.
    Harper PS
    Prog Clin Biol Res; 1989; 306():29-49. PubMed ID: 2567999
    [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]
    of 5.