46 xx

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Gastón Rey Valzacch
Sección de Andrología. Servicio de Urología. Hospital Italiano de Buenos Aires, Argentina

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Published: 2008-12-10
DOI: https://doi.org/10.51987/Rev.Hosp.Ital.B.Aires.v28i2.1079

Article Details

Issue

Vol. 28 No. 2 (2008): Revista del Hospital Italiano de Buenos Aires

Section

Clinical case
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This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License.

How to Cite

1.
Rey Valzacch G. 46 xx. Rev Hosp Ital B.Aires [Internet]. 2008 Dec. 10 [cited 2026 Jul. 31];28(2):75-6. Available from: https://ojs.hospitalitaliano.org.ar/index.php/revistahi/article/view/1079

References

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Bouayed Abdelmoula N, Portnoi MF. Keskes L, et al. Skewed X-chromosome inactivation pattern in SRY positive XX maleness: a case report and review of literature. Ann Genet. 2003;46(1):11-8.

Kusz K, Kotecki M, Wojda A, et al. Incomplete masculinisation of XX subjects carrying the SRY gene on an inactive X chromosome. J Med Genet. 1999;36(6):452-6.

McElreavey K, Cortes LS. X-Y translocations and sex differentiation. Semin Reprod Med. 2001;19(2):133-9.

Mittwoch U. Sex determination and sex reversal: genotype, phenotype, dogma and semantics. Hum Genet. 1992;89(5):467-79.

Schlegel PN. Causes of azoospermia and their management. Reprod Fertil Dev. 2004;16(5):561-72

Tomomasa H, Adachi Y, Iwabuchi M, et al XX-male syndrome bearing the sex-determining region Y. Arch Androl. 1999;42(2):89-96