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Journal Abstract Search

176 related items for PubMed ID: 3777018

  • 1. DUCHEN: an interactive computer program for calculating heterozygosity (carrier) risks in X-linked recessive lethal diseases, and its application in Duchenne muscular dystrophy.
    Andrews DF, Brasher PM, Manchester KE, Percy ME, Rusk AC, Soltan HC, Trueman DW.
    Am J Med Genet; 1986 Oct; 25(2):211-8. PubMed ID: 3777018
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  • 4. Complex segregation analysis and computer-assisted genetic risk assessment for Duchenne muscular dystrophy.
    Williams WR, Thompson MW, Morton NE.
    Am J Med Genet; 1983 Feb; 14(2):315-33. PubMed ID: 6837627
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  • 6. 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
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  • 11. Screening of male patients with autosomal recessive Duchenne dystrophy through dystrophin and DNA studies.
    Vainzof M, Pavanello RC, Pavanello-Filho I, Rapaport D, Passos-Bueno MR, Zubrzycka-Gaarn EE, Bulman DE, Zatz M.
    Am J Med Genet; 1991 Apr 01; 39(1):38-41. PubMed ID: 1867262
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  • 14. Duchenne muscular dystrophy carrier detection using logistic discrimination: serum creatine kinase, hemopexin, pyruvate kinase, and lactate dehydrogenase in combination.
    Percy ME, Andrews DF, Thompson MW.
    Am J Med Genet; 1982 Sep 01; 13(1):27-38. PubMed ID: 7137219
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  • 15. Improved detection of Duchenne muscular dystrophy heterozygotes using discriminant analysis of creatine kinase levels.
    Muir WA, Knoke J, Martin A, Vignos P, McErlean A.
    Am J Med Genet; 1983 Jan 01; 14(1):125-34. PubMed ID: 6829600
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  • 18. Serum myoglobin in Duchenne muscular dystrophy carrier detection: a comparison with creatine kinase and hemopexin using logistic discrimination.
    Percy ME, Pichora GA, Chang LS, Manchester KE, Andrews DF.
    Am J Med Genet; 1984 Jun 01; 18(2):279-87. PubMed ID: 6465202
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