Possible partial trisomy of a chromosome of group 6-X-12 and familial translocation heterozygosity in a child with congenital abnormalities.

Developmental medicine and child neurology ·Vol. 9 ·No. 3 ·1967-06-00 ·Pages 313-8

Jensen MK, Melchior JC

Abstract

暂无摘要

MeSH Terms

Chromosome Aberrations Chromosome Disorders Congenital Abnormalities Humans Infant Infant, Newborn Karyotyping Male Trisomy

Authors & Affiliations

2 authors, click to expand affiliations / ORCID

Jensen M K

Melchior J C

Article Info

Journal

Developmental medicine and child neurology

Abbr.

Dev Med Child Neurol

ISSN

0012-1622

DOI

Published

1967-06-00

Pages

313-8

Language

English

Region

England

NLM ID

0006761

Subset

External Links

Analysis Services