[Prenatal diagnosis of genetic diseases. Indications, methods, legal and ethic aspects. Neonatal screening of phenylketonuria and hypothyroidism].
作者信息
Farriaux J P
机构信息
Service de pédiatrie, hôpital J. de Flandre, Lille.
出版信息
Rev Prat. 1997 Dec 1;47(19):2159-68.
PMID:9501609
Abstract
摘要
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