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PMID: 569552 Published · ppublish English Case Reports Journal Article

Recessive sex-determining genes in human XX male syndrome.

Cell ·Vol. 15 ·No. 3 ·1978-11-00 ·Pages 837-42

de la Chapelle A, Koo GC, Wachtel SS

Abstract

Maleness is normally inherited as a dominant trait (a single copy of the Y chromosome induces testicular differentiation of the embryonic gonad), but our genealogic study of three XX males in one pedigree indicated an autosomal recessive mode of male inheritance. Subsequent study revealed the presence of H-Y antigens in the three XX males and in their mothers, and suggested that excess H-Y may be found in the fathers. Inasmuch as H-Y loci have been mapped to the human Y chromosome, these data favor the view that H-Y structural loci comprise a family of testis-determining genes, and that Y autosome (or Y-X) translocation can generate either dominant or recessive modes of XX sex reversal, depending upon the particular portion of H-Y genes transferred.

MeSH Terms
Adolescent Adult Disorders of Sex Development/genetics Female Genes, Recessive H-Y Antigen/genetics Humans Male Pedigree Syndrome X Chromosome
Chemicals
H-Y Antigen
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
de la Chapelle A
Koo G C
Wachtel S S
Article Info
Journal
Cell
Abbr.
Cell
ISSN
0092-8674
Published
1978-11-00
Pages
837-42
Language
English
Region
United States
NLM ID
0413066
Subset
IM
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