Comprehensive clinical and molecular studies in split-hand/foot malformation: identification of two plausible candidate genes (LRP6 and UBA2)
Kaori Yamoto(Hamamatsu University School of Medicine), Tsutomu Ogata(Hamamatsu University School of Medicine), Shiro Ikegawa(RIKEN Center for Integrative Medical Sciences), Rika Kosaki(National Center For Child Health and Development), Akihisa Okumura(Aichi Medical University), Emiko Horii(Japanese Red Cross Nagoya Daiichi Hospital), Fumiko Kato(National Center For Child Health and Development), Gen Nishimura(Musashino University), Hiroshi Suzumura(Dokkyo Medical University), Yasuko Fujisawa(Kobe University Hospital), Nobuhiko Haga(Boston Children's Hospital), Maki Fukami(National Center For Child Health and Development), Shuji Takada(National Center For Child Health and Development), Hirotomo Saitsu(Hamamatsu University), Hidefumi Tonoki(Sapporo University), Nobuhiko Okamoto(Osaka Women's and Children's Hospital), Shinichiro Takayama(National Center For Child Health and Development), Eiko Nagata(Hamamatsu University)
Cited by 18
Related Papers
Rationale and study design of the Japan environment and children’s study (JECS)
|BMC Public Health|2014|852
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
Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases
|Nature Genetics|2020|599
Nosology and classification of genetic skeletal disorders: 2015 revision
|American Journal of Medical Genetics Part A|2015|570