46, XY, t(3;22) (p2;q13) resulting in partial trisomy for the short arm of chromosome 3.

Clinical genetics ·Vol. 11 ·No. 3 ·1977-03-00 ·Pages 201-6

Surana RB, Braudo ME, Conen PE, Slade RH

Abstract

暂无摘要

MeSH Terms

Abnormalities, Multiple/genetics Adult Child, Preschool Chromosome Aberrations Chromosomes, Human, 1-3 Chromosomes, Human, 21-22 and Y Female Humans Infant Infant, Newborn Karyotyping Male Sex Chromosomes Translocation, Genetic Trisomy

Authors & Affiliations

4 authors, click to expand affiliations / ORCID

Surana R B

Braudo M E

Conen P E

Slade R H

Article Info

Journal

Clinical genetics

Abbr.

Clin Genet

ISSN

0009-9163

DOI

10.1111/j.1399-0004.1977.tb01300.x

Published

1977-03-00

Pages

201-6

Language

English

Region

Denmark

NLM ID

0253664

Subset

External Links

PubMed source DOI: 10.1111/j.1399-0004.1977.tb01300.x View journal details

Analysis Services

46, XY, t(3;22) (p2;q13) resulting in partial trisomy for the short arm of chromosome 3.

Contact

WeChat Official Account