Prenatal diagnosis of Duchenne muscular dystrophy by radio-immunoassay of myoglobin in amniotic fluid
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1982.tb01385.x/fullpdf
Reference3 articles.
1. Myoglobinaemia in Duchenne muscular dystrophy patients and carriers: a new adjunct to carrier detection;Adornato;Lancet,1978
2. Fetal serum-creatine-phosphokinase not a valid predictor of Duchenne muscular dystrophy;Ionasescu;Lancet,1978
3. Potential of radioim-munoassay of myoglobin in amniotic fluid and serum in prenatal diagnosis of Duchenne muscular dystrophy;Narregaard-Hansen;Lancet,1978
Cited by 6 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Plasma/serum myoglobin in prenatal diagnosis of duchenne muscular dystrophy;American Journal of Medical Genetics;1986-10
2. Plasma/serum myoglobin in prenatal diagnosis of duchenne muscular dystrophy;American Journal of Medical Genetics;1985-07
3. Elevated Second Trimester Amniotic Fluid Myoglobin from a Fetus with Duchenne Muscular Dystrophy;The Australian and New Zealand Journal of Obstetrics and Gynaecology;1985-05
4. Serum myoglobin in Duchenne muscular dystrophy carrier detection: A comparison with creatine kinase and hemopexin using logistic discrimination;American Journal of Medical Genetics;1984-06
5. The diagnostic value of plasma myoglobin levels in the adult and fetus at-risk for Duchenne muscular dystrophy;Journal of the Neurological Sciences;1984-02
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