How to cite this article: Shimizu R, Mitsui N, Mori Y, Cho S, Yamamori S, Osawa M, Ohashi H. 2008. Cryptic 17q22 deletion in a boy with a t(10;17)(p15.3;q22) translocation, multiple synostosis syndrome 1, and hypogonadotropic hypogonadism. Am J Med Genet Part A 146A:1458–1461.
Cryptic 17q22 deletion in a boy with a t(10;17)(p15.3;q22) translocation, multiple synostosis syndrome 1, and hypogonadotropic hypogonadism†
Version of Record online: 30 APR 2008
Copyright © 2008 Wiley-Liss, Inc.
American Journal of Medical Genetics Part A
Volume 146A, Issue 11, pages 1458–1461, 1 June 2008
How to Cite
Shimizu, R., Mitsui, N., Mori, Y., Cho, S., Yamamori, S., Osawa, M. and Ohashi, H. (2008), Cryptic 17q22 deletion in a boy with a t(10;17)(p15.3;q22) translocation, multiple synostosis syndrome 1, and hypogonadotropic hypogonadism. Am. J. Med. Genet., 146A: 1458–1461. doi: 10.1002/ajmg.a.32319
- Issue online: 19 MAY 2008
- Version of Record online: 30 APR 2008
- Manuscript Accepted: 20 FEB 2008
- Manuscript Received: 30 MAY 2007
- Ministry of Health, Labour and Welfare of Japan. Grant Number: H18-005
- Kawano Masanori Memorial Foundation for Promotion of Pediatrics, Japan
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