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PMID: 511193 Published · ppublish English Case Reports Journal Article

A familial extra small marker autosome in persons with normal phenotype.

Human heredity ·Vol. 29 ·No. 6 ·1979-00-00 ·Pages 371-3

Fried K, Rosenblatt M

Abstract

The propositus was referred because of sterility and oligospermia. His karyotype was 45, XY, t(13q14q). His father was dead; his mother and the only brother, who was fertile, both had 47 chromosomes, but a normal phenotype and normal intelligence. The additional chromosome was three quarters the size of a G chromosome and had satellites on the short and long arms.

MeSH Terms
Adult Chromosome Aberrations/genetics Chromosome Banding Chromosome Disorders Chromosomes, Human, 13-15 Chromosomes, Human, 21-22 and Y Humans Male Oligospermia/genetics Translocation, Genetic
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Fried K
Rosenblatt M
Article Info
Journal
Human heredity
Abbr.
Hum Hered
ISSN
0001-5652
Published
1979-00-00
Pages
371-3
Language
English
Region
Switzerland
NLM ID
0200525
Subset
IM
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