46 xx

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Gastón Rey Valzacch

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Rey Valzacch G. 46 xx. Rev Hosp Ital B.Aires [Internet]. 2008 Dec. 10 [cited 2026 Apr. 26];28(2):75-6. Available from: https://ojs.hospitalitaliano.org.ar/index.php/revistahi/article/view/1079

Referencias

Bhasin S. Approach to the infertile man. J Clin Endocrinol Metab. 2007;92(6):1995-2004. DOI: https://doi.org/10.1210/jc.2007-0634

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. DOI: https://doi.org/10.1016/S0003-3995(03)00011-X

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. DOI: https://doi.org/10.1136/jmg.36.6.452

McElreavey K, Cortes LS. X-Y translocations and sex differentiation. Semin Reprod Med. 2001;19(2):133-9. DOI: https://doi.org/10.1055/s-2001-15393

Mittwoch U. Sex determination and sex reversal: genotype, phenotype, dogma and semantics. Hum Genet. 1992;89(5):467-79. DOI: https://doi.org/10.1007/BF00219168

Schlegel PN. Causes of azoospermia and their management. Reprod Fertil Dev. 2004;16(5):561-72 DOI: https://doi.org/10.1071/RD03087

Tomomasa H, Adachi Y, Iwabuchi M, et al XX-male syndrome bearing the sex-determining region Y. Arch Androl. 1999;42(2):89-96 DOI: https://doi.org/10.1080/014850199262922