Home LiteratureArticle Details
PMID: 10931401 Published · ppublish English Comment Editorial

The 22q11.2 deletion syndrome: more answers but more questions.

The Journal of pediatrics ·Vol. 137 ·No. 2 ·2000-08-00 ·Pages 145-7

Fernhoff PM

Abstract

暂无摘要

MeSH Terms
Abnormalities, Multiple/diagnosis,epidemiology,genetics Adult Child Chromosome Deletion Chromosomes, Human, Pair 22 DiGeorge Syndrome/diagnosis,epidemiology,genetics Humans Infant Phenotype Syndrome
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Fernhoff P M
Article Info
Journal
The Journal of pediatrics
Abbr.
J Pediatr
ISSN
0022-3476
DOI
10.1067/mpd.2000.109024
Published
2000-08-00
Pages
145-7
Language
English
Region
United States
NLM ID
0375410
Subset
IM
Corrections
CommentOn
PMID: 10931405
CommentOn
PMID: 10931419
External Links
PubMed source DOI: 10.1067/mpd.2000.109024 View journal details
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