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A molecular deletion study with southern hybridization on typical Prader-Willi syndrome (PWS) patients with various chromosome abnormalities involving 15q11–12 and on an atypical PWS patient with apparently normal karyotype

✍ Scribed by Tsutomu Kamei; Jun-ichi Hamabe; Tadashi Matsumoto; Kyohko Abe; Naoki Harada; Satoshi Ishikiriyama; Tomoko Hasegawa; Kiyoshi Miyazaki; Seiji Mizuno; Kouji Narahara; Shigenori Yukizane; Norio Niikawa


Book ID
105393584
Publisher
Nature Publishing Group
Year
1988
Tongue
English
Weight
938 KB
Volume
33
Category
Article
ISSN
1435-232X

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