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PMID: 6700105 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Prenatal diagnosis of classical phenylketonuria by gene mapping.

JAMA ·Vol. 251 ·No. 15 ·1984-04-20 ·Pages 1998-2002

Woo SL, Lidsky AS, Güttler F, Thirumalachary C, Robson KJ

Abstract

暂无摘要

MeSH Terms
Chromosome Mapping Female Genetic Carrier Screening Humans Phenylalanine Hydroxylase/genetics Phenylketonurias/diagnosis,genetics,prevention & control Polymorphism, Genetic Pregnancy Prenatal Diagnosis
Chemicals
Phenylalanine Hydroxylase
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Woo S L
Lidsky A S
Güttler F
Thirumalachary C
Robson K J
Article Info
Journal
JAMA
Abbr.
JAMA
ISSN
0098-7484
Published
1984-04-20
Pages
1998-2002
Language
English
Region
United States
NLM ID
7501160
Subset
IM
Grants
NICHD NIH HHS · HD-17711 · United States
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