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PMID: 3411398 Published · ppublish English Case Reports Journal Article

Confirmation of autosomal dominant transmission of the DiGeorge malformation complex.

The Journal of pediatrics ·Vol. 113 ·No. 3 ·1988-09-00 ·Pages 506-8

Keppen LD, Fasules JW, Burks AW, Gollin SM, Sawyer JR, Miller CH

Abstract

暂无摘要

MeSH Terms
Adult Chromosome Deletion Chromosomes, Human, Pair 22 DiGeorge Syndrome/genetics Female Genes, Dominant Humans Immunologic Deficiency Syndromes/genetics Infant, Newborn Karyotyping Male
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Keppen L D
Department of Pediatrics, University of Arkansas for Medical Sciences, Little Rock.
Fasules J W
Burks A W
Gollin S M
Sawyer J R
Miller C H
Article Info
Journal
The Journal of pediatrics
Abbr.
J Pediatr
ISSN
0022-3476
DOI
10.1016/s0022-3476(88)80640-1
Published
1988-09-00
Pages
506-8
Language
English
Region
United States
NLM ID
0375410
Subset
IM
External Links
PubMed source DOI: 10.1016/s0022-3476(88)80640-1 View journal details
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