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PMID: 6176867 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Improved detection of the sickle mutation by DNA analysis: application to prenatal diagnosis.

The New England journal of medicine ·Vol. 307 ·No. 1 ·1982-07-01 ·Pages 32-6

Orkin SH, Little PF, Kazazian HH, Boehm CD

Abstract

暂无摘要

MeSH Terms

Anemia, Sickle Cell/diagnosis Base Sequence Beta-Globulins/genetics DNA/analysis DNA Restriction Enzymes Deoxyribonucleases, Type II Site-Specific Female Genetic Linkage Humans Male Nucleic Acid Hybridization Polymorphism, Genetic Pregnancy Prenatal Diagnosis/methods

Chemicals

Beta-Globulins DNA DNA Restriction Enzymes endodeoxyribonuclease MstII Deoxyribonucleases, Type II Site-Specific

Authors & Affiliations

4 authors, click to expand affiliations / ORCID

Orkin S H

Little P F

Kazazian H H

Boehm C D

Article Info

Journal

The New England journal of medicine

Abbr.

N Engl J Med

ISSN

0028-4793

DOI

10.1056/NEJM198207013070106

Published

1982-07-01

Pages

32-6

Language

English

Region

United States

NLM ID

0255562

Subset

Grants

NIADDK NIH HHS · AM 13983 · United States

NHLBI NIH HHS · HL 23689 · United States

External Links

PubMed source DOI: 10.1056/NEJM198207013070106 View journal details

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Improved detection of the sickle mutation by DNA analysis: application to prenatal diagnosis.

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