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Sex-reversed mice: XX and XO males

Cattanach, B.M., Pollard, C.E., Hawkes, S.G.·1971·Cytogenetic and Genome Research

Abstract

An autosomally inherited condition is described in the mouse which causes genetic females to develop as phenotypic males. XX males are phenotypically normal with the exception of small testes, which, in the adult, are devoid of germ cells. During late fetal and early postnatal development, male-type germ cells are present but progressively become lost, so that none is present by 10 days of age. XO males are also phenotypically normal, but spermatogenesis is active in the testis, and spermatozoa are produced. Cytological evidence of a Y-autosome translocation was completely lacking, and it is proposed that an autosomal dominant gene mutation, analogous to that found in other mammalian species, is responsible for the sex reversal.

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Metadata

Authors
Cattanach, B. M., Pollard, C. E., & Hawkes, S. G.
Venue
Cytogenetic and Genome Research
Publisher
S. Karger AG
Published
1971
Volume
10
Issue
5
Pages
318-337
ISSN
  • 0011-4537 (ISSN-L)
  • 1424-8581
  • 1424-859X
OpenAlex
W2067935567
Cited by
352
References
0
FWCI
1.58
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Sex-reversed mice: XX and XO males. https://app.cochat.ai/papers/10.1159/000130151
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Cattanach, B. M., Pollard, C. E., & Hawkes, S. G. (1971). Sex-reversed mice: XX and XO males. Cytogenetic and Genome Research. https://doi.org/10.1159/000130151

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