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J-GLOBAL ID:201702235911180339   Reference number:17A0580452

A case of 45,X/46,X,r (Y) mixed gonadal dysgenesis presenting with coarctation of the aorta

大動脈縮窄症を合併した45,X/46,X,r(Y)混合性性腺異形成症の1例
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Volume: 53  Issue:Page: 239-243  Publication year: May. 01, 2017 
JST Material Number: Z0500B  ISSN: 1348-964X  Document type: Article
Article type: 原著論文  Country of issue: Japan (JPN)  Language: JAPANESE (JA)
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Gynecologic and obstetric diagnosis 
Reference (13):
  • 長谷川行洋:性分化疾患.たのしく学ぶ小児内分泌.診断と治療社,2015:326-332
  • 藤枝憲二:性分化異常症,標準小児科学.医学書院, 2009:255-258
  • Milenkovic T, Guc-Scekic M, Zdravkovic D, et al. : Molecular analysis of ring Y chromosome in a 10-year-old boy with mixed gonadal dysgenesis and growth hormone deficiency. Balkan J Med Genet 2011 ; 14 (2) : 71-76
  • Hughes IA, Houk C, Ahmed SF, et al.: Consensus statement on management of intersex disorders. Arch Dis Child. 2006 ; 91 (7) : 554-563
  • Chang HJ, Clark RD, Bachman H : The phenotype of 45,X/46,XY mosaicism. Am J Hum Genet 1990 ; 46 : 156-167
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