[O17] Oral Session 17　Rare Diseases

[O17-3] Comprehensive analysis of Coffin-Siris syndrome with unresolved exome sequencing

Naomi Tsuchida¹, Yuri Uchiyama^1,2, Nobuhiko Okamoto³, Seiji Mizuno⁴, Kohei Hamanaka¹, Yukina Hayashi¹, Atsushi Fujita¹, Eriko Koshimizu¹, Satoko Miyatake^1,5, Takeshi Mizuguchi¹, Naomichi Matsumoto^1,2,5 (1.Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan, 2.Department of Rare Disease Genomics, Yokohama City University Hospital, Yokohama, Japan, 3.Department of Medical Genetics, Osaka Womenʼs and Childrenʼs Hospital, Osaka, Japan, 4.Department of Pediatrics, Central Hospital, Aichi Developmental Disability Center, Kasugai, Japan, 5.Clinical Genetics Department, Yokohama City University Hospital, Yokohama, Kanagawa, Japan)

Password required to view

Log in

or