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Journal Abstract Search

578 related items for PubMed ID: 7284070

  • 1. [Estimation of the probability of heterozygosity in Duchenne-type progressive muscular dystrophy].
    Guízar Vázquez J, Navarrete Cadena C, Rico R, Mora G, Zavala C.
    Bol Med Hosp Infant Mex; 1981; 38(1):23-33. PubMed ID: 7284070
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  • 2. [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
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  • 3. Use of normal daughters' and sisters' creatine kinase levels in estimating heterozygosity in Duchenne muscular dystrophy.
    Emery AE, Holloway S.
    Hum Hered; 1977 Nov 19; 27(2):118-26. PubMed ID: 863458
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  • 4. 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 19; 25(2):211-8. PubMed ID: 3777018
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  • 7. 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 19; 14(1):125-34. PubMed ID: 6829600
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  • 9. Creatine-phosphokinase (CPK) activity in relatives of patients with X-linked muscular dystrophies: a Brazilian study.
    Zatz M, Frota-Pessoa O, Levy JA, Peres CA.
    J Genet Hum; 1976 Jun 19; 24(2):153-68. PubMed ID: 965952
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  • 10. Genetic counseling of isolated carriers of Duchenne muscular dystrophy.
    Hoffman EP, Pegoraro E, Scacheri P, Burns RG, Taber JW, Weiss L, Spiro A, Blattner P.
    Am J Med Genet; 1996 Jun 28; 63(4):573-80. PubMed ID: 8826437
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  • 11. Estimate of the proportion of Duchenne muscular dystrophy with autosomal recessive inheritance.
    Zatz M, Passos-Bueno MR, Rapaport D.
    Am J Med Genet; 1989 Mar 28; 32(3):407-10. PubMed ID: 2658592
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  • 12. Comparison of serum creatine kinase estimation with short tandem repeats based linkage analysis in carriers and affected children of Duchenne muscular dystrophy.
    Hashim R, Shaheen S, Ahmad S, Sattar A, Khan FA.
    J Ayub Med Coll Abbottabad; 2011 Mar 28; 23(1):125-8. PubMed ID: 22830166
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  • 14. [Carrier detection and gene analysis in a Duchenne muscular dystrophy family].
    Lu FM.
    Zhonghua Shen Jing Jing Shen Ke Za Zhi; 1990 Aug 28; 23(4):231-3, 255. PubMed ID: 1979269
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  • 16. Duchenne muscular dystrophy carrier detection using logistic discrimination: serum creatine kinase and hemopexin in combination.
    Percy ME, Andrews DF, Thompson MW.
    Am J Med Genet; 1981 Aug 28; 8(4):397-409. PubMed ID: 7246612
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  • 19. [Muscle LDH isoenzymes in neuromuscular diseases and in carriers of recessive X-linked muscular dystrophy (duchenne)].
    Kowalewski S, Rotthauwe HW.
    Z Kinderheilkd; 1972 Aug 28; 113(1):55-70. PubMed ID: 5056500
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  • 20. 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 28; 25(2):219-30. PubMed ID: 3777019
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