[2P-2] Poster Presentation

4. 高次生命現象・疾患 - l. 遺伝性疾患

[2P-916] Statistical results of a comprehensive genomic analysis of 1,560 patients with rare or undiagnosed diseases at a single centre

○Tadashi Kaname^1,2,7, Kumiko Yanagi^1,7, Arisa Igarashi¹, Taiga Aoki¹, Takaya Iida¹, Masahiko Yamamori¹, Kazuhito Satou¹, Yasutsugu Chinen^3,7, Yoko Aoki^4,7, Ko-ichiro Yoshiura^5,7, Nobuhiko Okamoto^6,7, NCCHD GM consortium IRUD⁷, Yoichi Matsubara^1,7 (1. Department of Genome Medicine, National Center for Child Health and Development, 2. Allergy Center, NCCHD, 3. Dept Ped, Grad Schl Med, Univ Ryukyus, 4. Dept Med Genet, Tohoku Univ Schl Med, 5. Dept Hum Genet, Nagasaki Univ Grad Schl Biomed Sci, 6. Dept Med Genet, OWCH, 7. IRUD NCCHD-GM consortium)

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