Detection of carriers for duchenne muscular dystrophy. Quality control of creatine kinase assay

[1]  M. Zatz,et al.  Effect of age on the detection rate in Duchenne muscular dystrophy , 1980, Journal of the Neurological Sciences.

[2]  T. Whitehead,et al.  SERUM CREATINE KINASE ACTIVITY AND CARRIER STATUS FOR DUCHENNE MUSCULAR DYSTROPHY , 1979, The Lancet.

[3]  M. W. Thompson,et al.  Serum creatine kinase and pyruvate kinase in duchenne muscular dystrophy carrier detection , 1979, Muscle & nerve.

[4]  V. Dubowitz,et al.  ANTENATAL DIAGNOSIS OF DUCHENNE MUSCULAR DYSTROPHY , 1979, The Lancet.

[5]  J. Hobbins,et al.  Failure of fetal creatine phosphokinase as a diagnostic indicator of Duchenne muscular dystrophy. , 1979, The New England journal of medicine.

[6]  A. Emery,et al.  Serum LDH‐5 in carriers of Duchenne muscular dystrophy , 1979, Neurology.

[7]  A. Davie,et al.  Estimation of proportion of new mutants among cases of Duchenne muscular dystrophy. , 1978, Journal of medical genetics.

[8]  H. Kawai,et al.  Radioimmunoassay for human myoglobin: methods and results in patients with skeletal muscle or myocardial disorders. , 1978, The Journal of laboratory and clinical medicine.

[9]  A. Roses,et al.  Lactate dehydrogenase isoenzyme 5 in detecting carriers of Duchenne muscular dystrophy , 1977, Neurology.

[10]  V. Ionasescu,et al.  DETECTION of CARRIERS and GENETIC COUNSELING IN DUCHENNE MUSCULAR DYSTROPHY BY RIBOSOMAL PROTEIN SYNTHESIS , 1976, Acta neurologica Scandinavica.

[11]  I. Strøyer,et al.  C1-ESTERASE INACTIVATORS AND C4 IN MALIGNANT DISEASES , 1975, The Lancet.

[12]  MiriamG. Wilson,et al.  46,XX/47,XYY MOSAICISM IN A TRUE HERMAPHRODITE , 1975, The Lancet.

[13]  Vladutiu Ao Letter: C3 standards? , 1975 .

[14]  V. Dubowitz,et al.  Carrier detection in Duchenne muscular dystrophy. A comparative study of electron microscopy, light microscopy and serum enzymes. , 1970, Journal of the neurological sciences.

[15]  H. Hartley,et al.  Maximum-likelihood estimation for the mixed analysis of variance model. , 1967, Biometrika.

[16]  M. W. Thompson,et al.  Duchenne muscular dystrophy carrier detection using logistic discrimination: serum creatine kinase and hemopexin in combination. , 1981, American journal of medical genetics.

[17]  T. Kato,et al.  Myoglobinemia in Duchenne muscular dystrophy carriers. , 1980, Brain & development.

[18]  N. Morton,et al.  Genetic counseling in sex linkage. , 1979, Birth defects original article series.

[19]  B. Goldsmith,et al.  Lymphocyte capping in Duchenne muscular dystrophy. , 1979, Lancet.

[20]  J. Hamerton,et al.  Report of the committee on the genetic constitution of chromosome 1. , 1979, Cytogenetics and cell genetics.