Prenatal diagnosis of glutaryl-CoA dehydrogenase deficiency: Experience using first-trimester chorionic villus sampling
Author:
Publisher
Wiley
Subject
Genetics(clinical),Obstetrics and Gynaecology
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5. Disorders of Ornithine, Lysine and Tryptophan;Physician’s Guide to the Laboratory Diagnosis of Metabolic Diseases;2003
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