Partial trisomy of chromosome 22 resulting from an interstitial duplication of 22q11.2 in a child with typical cat eye syndrome.

Journal of medical genetics ·Vol. 40 ·No. 5 ·2003-05-00 ·Pages e62

Meins M, Burfeind P, Motsch S, Trappe R, Bartmus D, Langer S, Speicher MR, Mühlendyck H, Bartels I, Zoll B

Abstract

暂无摘要

MeSH Terms

Abnormalities, Multiple/genetics,pathology Chromosomes, Human, Pair 22/genetics Eye Abnormalities/genetics,pathology Gene Duplication Humans Infant Infant, Newborn Male Phenotype Syndrome Trisomy/genetics

Authors & Affiliations

10 authors, click to expand affiliations / ORCID

Meins M

Burfeind P

Motsch S

Trappe R

Bartmus D

Langer S

Speicher M R

Mühlendyck H

Bartels I

Zoll B

Article Info

Journal

Journal of medical genetics

Abbr.

J Med Genet

ISSN

1468-6244

DOI

10.1136/jmg.40.5.e62

Published

2003-05-00

Pages

e62

Language

English

Region

England

NLM ID

2985087R

PMCID

PMC1735484

Subset

External Links

PubMed source DOI: 10.1136/jmg.40.5.e62 PMC Full Text View journal details

Analysis Services

Partial trisomy of chromosome 22 resulting from an interstitial duplication of 22q11.2 in a child with typical cat eye syndrome.

Contact

WeChat Official Account