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32. [Genetics and clinical types of progressive muscular dystrophy; creatine kinase and myoglobin as biochemical indices of the disease]. Miyoshi K; Kawai H; Sasaki H; Iwaasa M; Yagita M; Ise H; Kondo A; Hiasa M Nihon Rinsho; 1977 Nov; 35(11):3891-6. PubMed ID: 599669 [No Abstract] [Full Text] [Related]
33. Myoglobinaemia in Duchenne muscular dystrophy patients and carriers: A new adjunct to carrier detection. Adornato BT; Kagen LJ; Engel WK Lancet; 1978 Sep; 2(8088):499-501. PubMed ID: 79868 [TBL] [Abstract][Full Text] [Related]
34. Estimates of conditional heterozygosity risks for young females in Duchenne muscular dystrophy. Passos-Bueno MR; Otto PA; Zata M Hum Hered; 1989; 39(4):202-11. PubMed ID: 2583732 [TBL] [Abstract][Full Text] [Related]
36. In utero fetal muscle biopsy for the diagnosis of Duchenne muscular dystrophy in a female fetus "suddenly at risk". Evans MI; Farrell SA; Greb A; Ray P; Johnson MP; Hoffman EP Am J Med Genet; 1993 May; 46(3):309-12. PubMed ID: 8488877 [TBL] [Abstract][Full Text] [Related]
37. Activity of creatine kinase in sera from healthy women, carriers of Duchenne muscular dystrophy and cord blood, determined by the "European" recommended method with NAC-EDTA activation. Moss DW; Whitaker KB; Parmar C; Heckmatt J; Wikowski J; Sewry C; Dubowitz V Clin Chim Acta; 1981 Oct; 116(2):209-16. PubMed ID: 6794955 [TBL] [Abstract][Full Text] [Related]