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PMID: 6607413 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Prenatal diagnosis of alpha 1-antitrypsin deficiency by direct analysis of the mutation site in the gene.

The New England journal of medicine ·Vol. 310 ·No. 10 ·1984-03-08 ·Pages 639-42

Kidd VJ, Golbus MS, Wallace RB, Itakura K, Woo SL

Abstract

暂无摘要

MeSH Terms

Chromosome Mapping DNA/analysis Female Heterozygote Homozygote Humans Male Mutation Nucleic Acid Hybridization Prenatal Diagnosis/methods alpha 1-Antitrypsin/genetics alpha 1-Antitrypsin Deficiency

Chemicals

alpha 1-Antitrypsin DNA

Authors & Affiliations

5 authors, click to expand affiliations / ORCID

Kidd V J

Golbus M S

Wallace R B

Itakura K

Woo S L

Article Info

Journal

The New England journal of medicine

Abbr.

N Engl J Med

ISSN

0028-4793

DOI

10.1056/NEJM198403083101007

Published

1984-03-08

Pages

639-42

Language

English

Region

United States

NLM ID

0255562

Subset

Grants

NHLBI NIH HHS · HL 27509 · United States

NHLBI NIH HHS · HL 29516 · United States

External Links

PubMed source DOI: 10.1056/NEJM198403083101007 View journal details

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Prenatal diagnosis of alpha 1-antitrypsin deficiency by direct analysis of the mutation site in the gene.

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