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PMID: 6221838 Published · ppublish English Case Reports Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Inherited 13/14 translocation and metacentric microchromosome associated with trisomy 21: report of 2 cases.

Clinical genetics ·Vol. 23 ·No. 5 ·1983-05-00 ·Pages 386-90

Leddet-Chevallier I, Sparkes RS

Abstract

暂无摘要

MeSH Terms

Adult Child Child, Preschool Chromosome Aberrations Chromosomes, Human, 13-15 Down Syndrome/genetics Female Genetic Markers Humans Infant, Newborn Male Pedigree Translocation, Genetic

Chemicals

Genetic Markers

Authors & Affiliations

2 authors, click to expand affiliations / ORCID

Leddet-Chevallier I

Sparkes R S

Article Info

Journal

Clinical genetics

Abbr.

Clin Genet

ISSN

0009-9163

DOI

10.1111/j.1399-0004.1983.tb00451.x

Published

1983-05-00

Pages

386-90

Language

English

Region

Denmark

NLM ID

0253664

Subset

Grants

NICHD NIH HHS · HD04612 · United States

NICHD NIH HHS · HD05615 · United States

External Links

PubMed source DOI: 10.1111/j.1399-0004.1983.tb00451.x View journal details

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Inherited 13/14 translocation and metacentric microchromosome associated with trisomy 21: report of 2 cases.

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