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PUBMED FOR HANDHELDS

Journal Abstract Search

82 related items for PubMed ID: 3621760

  • 1.
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  • 2. [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]

  • 3. Genetic counseling in Becker type X-linked muscular dystrophy. I. Theoretical considerations.
    Grimm T.
    Am J Med Genet; 1984 Aug; 18(4):713-8. PubMed ID: 6486169
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  • 5. [New aspects of carrier diagnosis and human genetic counseling in Duchenne and Becker muscular dystrophy].
    Spiegler AW, Huppert P, Werner W, Metzke H, Strobel U, Köhler K, Gerhardt R, Kaufmann J, Herrmann FH.
    Z Arztl Fortbild (Jena); 1988 Aug; 82(22):1139-42. PubMed ID: 3247797
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  • 8. 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
    [Abstract] [Full Text] [Related]

  • 9. Genetic counseling in Becker type X-linked muscular dystrophy. II: Practical considerations.
    Grimm T.
    Am J Med Genet; 1984 Aug; 18(4):719-23. PubMed ID: 6486170
    [Abstract] [Full Text] [Related]

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  • 13. [Identification of the carrier state in the severe recessive X-linked muscular dystrophy (Duchenne type). I. Assay of activated serum creatine kinase activity in serum (author's transl)].
    Rotthauwe HW, Kowalewski S.
    Z Kinderheilkd; 1973 Nov 19; 115(4):333-42. PubMed ID: 4591596
    [No Abstract] [Full Text] [Related]

  • 14. One family of benign X-linked pseudohypertrophic muscular dystrophy of early onset.
    Itoga E, Kito S.
    Hiroshima J Med Sci; 1984 Sep 19; 33(3):303-10. PubMed ID: 6542554
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  • 15. [X-linked progressive muscular dystrophies with early onset and contractures (review of the literature)].
    Badalian LO, Temin PA, Zavadenko NN.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1990 Sep 19; 90(3):123-8. PubMed ID: 2163153
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  • 16. Evaluation of carrier detection rates for Duchenne and Becker muscular dystrophies using serum creatine-kinase (CK) and pyruvate-kinase (PK) through discriminant analysis.
    Zatz M, Otto PA.
    Am J Med Genet; 1986 Oct 19; 25(2):219-30. PubMed ID: 3777019
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  • 17. Duchenne muscular dystrophy and idiopathic hyperCKemia in a family causing confusion in genetic counselling.
    Bushby K, Goodship J, Haggerty D, Heald A, Walls T.
    Am J Med Genet; 1996 Dec 11; 66(2):237-8. PubMed ID: 8958338
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  • 18. [Biochemical, histological and clinical findings in carriers of Duchenne-type progressive muscular dystrophy].
    Moser H, Mumenthaler M, Wiesmann U.
    Schweiz Med Wochenschr; 1971 Apr 17; 101(15):537-42. PubMed ID: 5576948
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  • 19. Duchenne muscular dystrophy in a female with 45,X/46,XX chromosome constitution.
    Sano M, Saito F, Yamamoto K, Tonomura A, Tsukagoshi H.
    Jinrui Idengaku Zasshi; 1987 Sep 17; 32(3):257-62. PubMed ID: 3448308
    [No Abstract] [Full Text] [Related]

  • 20. [Duchenne muscular dystrophy. Fragile X syndrome. Epidemiology, genetics, diagnosis].
    Pinson S, Plauchu H.
    Rev Prat; 1998 Mar 01; 48(5):565-9. PubMed ID: 9781124
    [No Abstract] [Full Text] [Related]

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