A 1/G translocation in a member of a kindred with a marker chromosome.

Archives of internal medicine ·Vol. 119 ·No. 3 ·1967-03-00 ·Pages 297-301

Maganias NH, Archambault L, Becker KL, Winnacker JL

Abstract

暂无摘要

MeSH Terms

Child, Preschool Chromosome Aberrations/genetics Chromosome Disorders Dermatoglyphics Female Humans Intellectual Disability Karyotyping

Authors & Affiliations

4 authors, click to expand affiliations / ORCID

Maganias N H

Archambault L

Becker K L

Winnacker J L

Article Info

Journal

Archives of internal medicine

Abbr.

Arch Intern Med

ISSN

0003-9926

Published

1967-03-00

Pages

297-301

Language

English

Region

United States

NLM ID

0372440

Subset

External Links

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