Presentation Information
[P2-08-11]Clinical characterization of a patient with chromosome 20p11.2 deletion syndrome
○Ryojun Takeda1,2, Yuma Shibuya3, Keisuke Nagasaki2,4, Kyoko Takano1,5,6, Keiko Wakui5,6, Tomoki Kosho1,5,6,7,8,9 (1.Department of Medical Genetics, Nagano Childrens Hospital, Azumino, Japan, 2.Life Science Research Center, Nagano Childrens Hospital, Azumino, Japan, 3.Department of Cardiology, Nagano Childrens Hospital, Azumino, Japan, 4.Department of Endocrinology and Metabolism, Nagano Childrens Hospital, Azumino, Japan, 5.Department of Medical Genetics, Shinshu University School of Medicine, Matsumoto, Japan, 6.Center for Medical Genetics, Shinshu University Hospital, Matsumoto, Japan, 7.Division of Clinical Sequencing, Shinshu University School of Medicine, Matsumoto, Japan, 8.Research Center for Advanced Science and Technology, Shinshu University, Matsumoto, Japan, 9.BioBank Shinshu, Shinshu University Hospital, Matsumoto, Japan)