Mutations in genes encoding polycomb repressive complex 2 subunits cause Weaver syndrome
Eri Imagawa(Yokohama City University), Naomichi Matsumoto(Yokohama City University), Nobuhiko Okamoto(Osaka Women's and Children's Hospital), Akihide Ryo(National Institute of Infectious Diseases), Chikahiko Numakura(Yamagata University), Satoko Matsunaga(Daiichi-Sankyo (Japan)), Satoko Miyatake(Shiga University of Medical Science), Gen Nishimura(Musashino University), Yasunari Sakai(Kyushu University), Yui Takada(Japanese Red Cross Fukuoka Hospital), Kenji Ihara(Oita University), Takeshi Mizuguchi(National Cancer Institute), Hidenobu Soejima(Saga University), Masafumi Sanefuji(Kyushu University), Mitsuko Nakashima(Hamamatsu University School of Medicine), Hirotomo Saitsu(Hamamatsu University), Noriko Miyake(National Center for Global Health and Medicine), Yoshinori Sato, Ken Higashimoto(Saga University)
Cited by 105
Related Papers
Nosology and classification of genetic skeletal disorders: 2010 revision
|American Journal of Medical Genetics Part A|2011|717
Nosology and classification of genetic skeletal disorders: 2019 revision
|American Journal of Medical Genetics Part A|2019|620
Nosology and classification of genetic skeletal disorders: 2015 revision
|American Journal of Medical Genetics Part A|2015|570
Nosology of genetic skeletal disorders: 2023 revision
|American Journal of Medical Genetics Part A|2023|386