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PMID: 1036513 Published · ppublish English Case Reports Journal Article Research Support, U.S. Gov't, P.H.S.

Y-chromosomal genes in a phenotypic male with a 46XX karyotype.

JAMA ·Vol. 236 ·No. 22 ·1976-11-29 ·Pages 2505-8

Dosik H, Wachtei SS, Khan F, Spergel G, Koo GC

Abstract

A number of patients with a male phenotype and a female (46XX) karyotype have been described. Although there is little or no evidence for the presence of a Y chromosome in their cells, these individuals resemble patients with Klinefelter syndrome (47XXY). Using a new serological assay for the presence of H-Y antigen, a cell surface component associated with the Y chromosome, we have demonstrated the presence of Y-chromosomal genes in a 46-year-old man with an XX karyotype. In addition, using standard cytological technique, we have located a minor population of XXY cells as well as cells bearing and abnormal chromosome 17 among the blood leukocytes of this individual.

MeSH Terms
Chromosomes, Human, 16-18 Disorders of Sex Development Genes Histocompatibility Antigens Humans Karyotyping Klinefelter Syndrome/genetics Male Mosaicism Mutation Phenotype Sex Chromosomes Translocation, Genetic
Chemicals
Histocompatibility Antigens
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Dosik H
Wachtei S S
Khan F
Spergel G
Koo G C
Article Info
Journal
JAMA
Abbr.
JAMA
ISSN
0098-7484
Published
1976-11-29
Pages
2505-8
Language
English
Region
United States
NLM ID
7501160
Subset
IM
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