The cri du chat syndrome in adolescents and adults: clinical finding in 13 older patients with partial deletion of the short arm of chromosome No. 5(5p-).

The Journal of pediatrics ·Vol. 77 ·No. 5 ·1970-11-00 ·Pages 782-91

Breg WR, Steele MW, Miller OJ, Warburton D, DeCapoa A, Allderdice PW

Abstract

暂无摘要

MeSH Terms

Abnormalities, Multiple/genetics Adolescent Adult Child Chromosomes, Human, 4-5 Craniofacial Dysostosis/genetics Cri-du-Chat Syndrome/genetics DNA Replication Female Heterozygote Humans Karyotyping Male Malocclusion/genetics Microcephaly/genetics Middle Aged Scoliosis/genetics Strabismus/genetics

Authors & Affiliations

6 authors, click to expand affiliations / ORCID

Breg W R

Steele M W

Miller O J

Warburton D

DeCapoa A

Allderdice P W

Article Info

Journal

The Journal of pediatrics

Abbr.

J Pediatr

ISSN

0022-3476

DOI

10.1016/s0022-3476(70)80236-0

Published

1970-11-00

Pages

782-91

Language

English

Region

United States

NLM ID

0375410

Subset

External Links

PubMed source DOI: 10.1016/s0022-3476(70)80236-0 View journal details

Analysis Services

The cri du chat syndrome in adolescents and adults: clinical finding in 13 older patients with partial deletion of the short arm of chromosome No. 5(5p-).

Contact

WeChat Official Account