Presentation Information
[P1-03-05]Whole-genome sequencing analysis of complex structural variants in 9p deletion and duplication syndrome
Suzuran Saito1, Eriko Koshimizu1, Atsushi Fujita1, Akihiko Miyauchi2, Naomi Tsuchida1,3, Yuri Uchiyama1,3, Masamune Sakamoto1, Kohei Hamanaka1, Satoko Miyatake1,4, Takeshi Mizuguchi1, Kenjiro Kosaki5, Hitoshi Osaka2, Naomichi Matsumoto1,3,4,6 (1. Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan, 2. Department of Pediatrics, Jichi Medical School, Shimotsuke, Tochigi, Japan, 3. Department of Rare Disease Genomics, Yokohama City University Hospital, Yokohama, Japan, 4. Department of Clinical Genetics, Yokohama City University Hospital, Yokohama, Japan, 5. Center for Medical Genetics, Keio University School of Medicine, Tokyo, Japan, 6. Medical Genome Center, National Center of Neurology and Psychiatry, Tokyo, Japan)
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