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A Case of 46 , XX Male

Kim JI, Rhee JH, Kang SS

  • KMID: 2261376
  • Korean J Obstet Gynecol.
  • 1999 Mar;42(3):628-631.
46, XX male is a rare sex cluomasomal constitution characterized by the development of bilateral testis in persons who lack a Y chomosome. The majority of affected persons have normal...
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Analysis of SRY Gene in Korean Patients with Swyer Syndrome and their Family Members

Chae HD, Choi YM, Lee JY

  • KMID: 2075242
  • Korean J Obstet Gynecol.
  • 1997 Jul;40(7):1419-1429.
Individuals affected with Swyer syndrome are phenotypic females with 46, XY karyotype, sexual infantilism, mullerina derivatives, and bilateral streak gonads that may undergo neoplastic transformation. The pathogenesis of this syndrome...
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A Case of a 46,XX Male with SRY Gene

Min J, Lee DS, Cho SK, Park S, Lee S, Baek M, Kim K, Hwang D

  • KMID: 2184461
  • J Genet Med.
  • 2008 Dec;5(2):145-149.
46,XX male is a rare sex constitution characterized by the development of bilateral testis in persons who lack a Y chromosome. Manifestations of 46,XX males are usually hypogonadism, gynecomastia, azoospermia,...
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Molecular Analysis of the Y Chromosome in a 46,XY Female Phenotype

Kim JW, Kim TJ, Park SY, Nam SA, Jun JY

  • KMID: 1536936
  • J Genet Med.
  • 1999 Dec;3(1):5-10.
This is a case report of 46,XY female phenotype (46,XY karyotype, no pubic hair, blind vagina and absence of uterus)in an 18-year-old patient. To confirm whether a Y chromosome has...
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