Partial trisomy 3q and the mild Cornelia de Lange syndrome phenotype.

Journal of medical genetics ·Vol. 32 ·No. 10 ·1995-10-00 ·Pages 837-8

Ireland M, English C, Cross I, Lindsay S, Strachan T

Abstract

暂无摘要

MeSH Terms

Child Chromosomes, Human, Pair 3 De Lange Syndrome/genetics Humans Phenotype Trisomy

Authors & Affiliations

5 authors, click to expand affiliations / ORCID

Ireland M

English C

Cross I

Lindsay S

Strachan T

References (1)

1 references, click to expand

Partial trisomy 3q causing mild Cornelia de Lange phenotype.
J Med Genet. 1994 Feb;31(2):150-2 PMID: 8182724

Article Info

Journal

Journal of medical genetics

Abbr.

J Med Genet

ISSN

0022-2593

DOI

Published

1995-10-00

Pages

837-8

Language

English

Region

England

NLM ID

2985087R

PMCID

PMC1051721

Subset

Corrections

CommentOn

PMID: 8182724

External Links

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