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Cryptic 17q22 deletion in a boy with a t(10;17)(p15.3;q22) translocation, multiple synostosis syndrome 1, and hypogonadotropic hypogonadism

✍ Scribed by Reiko Shimizu; Norimasa Mitsui; Yasuhiro Mori; Shogen Cho; Shunji Yamamori; Makiko Osawa; Hirofumi Ohashi

Publisher: John Wiley and Sons
Year: 2008
Tongue: English
Weight: 129 KB
Volume: 146A
Category: Article
ISSN: 1552-4825
DOI: 10.1002/ajmg.a.32319

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