Disorder of sex development in an infant with molecularly confirmed 46,XY, +der(10)t(10;21)(q21.1;q21.3), -21-Reference-Cited by-同舟云学术

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Disorder of sex development in an infant with molecularly confirmed 46,XY, +der(10)t(10;21)(q21.1;q21.3), -21

Published:2014-01-17 Issue:3 Volume:164 Page:841-843
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Yagasaki Hideaki¹,Nakane Takaya¹,Saito Tomohiro¹,Koizumi Keiichi¹,Kobayashi Kisho¹,Ogata Tsutomu²

Affiliation:

1. Department of Pediatrics; Faculty of Medicine, University of Yamanashi; Yamanashi Japan

2. Department of Pediatrics; Hamamatsu University School of Medicine; Hamamatsu Japan

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.36354/fullpdf

Reference12 articles.

1. Disorders of Sex Development

2. Pure trisomy 10p involving an isochromosome 10p;Berend;Clin Genet,1999

3. The Consequences of Chromosome Imbalance

4. Developmental and other pathologic changes in syndromes caused by chromosome abnormalities;Gilbert;Perspect Pediatr Pathol,1982

5. Consensus statement on management of intersex disorders;Hughes;Arch Dis Child,2006

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