Familial true hermaphroditism: paternal and maternal transmission of true hermaphroditism (46,XX) and XX maleness in the absence of Y-chromosomal sequences-Reference-Cited by-同舟云学术

Familial true hermaphroditism: paternal and maternal transmission of true hermaphroditism (46,XX) and XX maleness in the absence of Y-chromosomal sequences

Published:1993-12 Issue:6 Volume:92 Page:571-576
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Kuhnle U.,Schwarz H. P.,L�hrs U.,Stengel-Ruthkowski S.,Cleve H.,Braun A.

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/BF00420941.pdf

Reference31 articles.

1. Aaronson IA (1985) True hermaphroditism. A review of 41 cases with observations on testicular histology and function. Br J Urol 57:775?779

2. Abbas NE, Toublanc JE, Boucekkine C, Toublanc M, Affara NA, Job J-C, Fellous M (1990) A possible common origin of ?Y-negative? human XX-males and XX true hermaphrodites. Hum Genet 84:356?360

3. Affara NA (1991) Sex and the single Y. Bio Essays 13:475?478

4. Berkovitz GD, Fechner PY, Marcantonio SM, Bland G, Stetten G, Goodfellow PN, Smith KB, Migeon CJ (1992) The role of the sex-determining region of the Y chromosome (SRY) in the etiology of 46,XX true hermaphroditism. Hum Genet 88:411?416

5. Berta Ph, Hawkins JR, Sinclair AH, Taylor A, Griffiths BL, Goodfellow PN, Fellous M (1990) Genetic evidence equating SRY and the testis-determing factor. Nature 348:448?450

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