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Spread of X-chromosome inactivation into chromosome 15 is associated with Prader–Willi syndrome phenotype in a boy with a t(X;15)(p21.1;q11.2) translocation

✍ Scribed by Satoru Sakazume; Hirofumi Ohashi; Yuki Sasaki; Naoki Harada; Katsumi Nakanishi; Hidenori Sato; Mitsuru Emi; Kazushi Endoh; Ryoichi Sohma; Yasuhiro Kido; Toshiro Nagai; Takeo Kubota

Publisher: Springer
Year: 2011
Tongue: English
Weight: 758 KB
Volume: 131
Category: Article
ISSN: 0340-6717
DOI: 10.1007/s00439-011-1051-4

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