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PMID: 2880228 Published · ppublish English Case Reports Letter Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Prenatal diagnosis of medium-chain acyl-CoA dehydrogenase deficiency in family with sudden infant death.

Lancet (London, England) ·Vol. 1 ·No. 8530 ·1987-02-21 ·Pages 440-1

Bennett MJ, Allison F, Pollitt RJ, Manning NJ, Gray RG, Green A, Hale DE, Coates PM

Abstract

暂无摘要

MeSH Terms

Acyl-CoA Dehydrogenase Acyl-CoA Dehydrogenases/deficiency Amniotic Fluid/analysis Female Fetal Diseases/diagnosis Humans Infant Male Pregnancy Prenatal Diagnosis Sudden Infant Death

Chemicals

Acyl-CoA Dehydrogenases Acyl-CoA Dehydrogenase

Authors & Affiliations

8 authors, click to expand affiliations / ORCID

Bennett M J

Allison F

Pollitt R J

Manning N J

Gray R G

Green A

Hale D E

Coates P M

Article Info

Journal

Lancet (London, England)

Abbr.

Lancet

ISSN

0140-6736

DOI

10.1016/s0140-6736(87)90135-8

Published

1987-02-21

Pages

440-1

Language

English

Region

England

NLM ID

2985213R

Subset

Grants

NIADDK NIH HHS · AMO1226 · United States

NINDS NIH HHS · NS17752 · United States

External Links

PubMed source DOI: 10.1016/s0140-6736(87)90135-8 View journal details

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Prenatal diagnosis of medium-chain acyl-CoA dehydrogenase deficiency in family with sudden infant death.

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