Home LiteratureArticle Details
PMID: 3762643 Published · ppublish English Case Reports Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Prenatal diagnosis of ornithine transcarbamylase deficiency with use of DNA polymorphisms.

The New England journal of medicine ·Vol. 315 ·No. 19 ·1986-11-06 ·Pages 1205-8

Fox J, Hack AM, Fenton WA, Golbus MS, Winter S, Kalousek F, Rozen R, Brusilow SW, Rosenberg LE

Abstract

暂无摘要

MeSH Terms
Amino Acid Metabolism, Inborn Errors/diagnosis DNA/analysis Female Fetal Diseases/diagnosis Genetic Carrier Screening Humans Male Ornithine Carbamoyltransferase/genetics Ornithine Carbamoyltransferase Deficiency Disease Polymorphism, Genetic Pregnancy Prenatal Diagnosis
Chemicals
DNA Ornithine Carbamoyltransferase
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Fox J
Hack A M
Fenton W A
Golbus M S
Winter S
Kalousek F
Rozen R
Brusilow S W
Rosenberg L E
Article Info
Journal
The New England journal of medicine
Abbr.
N Engl J Med
ISSN
0028-4793
DOI
10.1056/NEJM198611063151907
Published
1986-11-06
Pages
1205-8
Language
English
Region
United States
NLM ID
0255562
Subset
IM
Grants
NIADDK NIH HHS · AM 12579 · United States
NIGMS NIH HHS · GM 32156 · United States
NICHD NIH HHS · HD 11134 · United States
External Links
PubMed source DOI: 10.1056/NEJM198611063151907 View journal details
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]

Copyright © 2026.Genelibs Jinan Honghui Biotechnology Co., Ltd. 鲁ICP备20007159号-2