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Norio Niikawa (新川 詔夫 Niikawa Norio?, born May 8, 1942) is a Japanese physician and medical geneticist who discovered an autosomal dominant disorder Kabuki syndrome, also known as Niikawa-Kuroki syndrome.[1] He and his colleagues also identified a gene for the syndrome.Niikawa completed his M.D. in 1967 from Hokkaido University School of Medicine.[3] After residency in Pediatrics at Hokkaido University Hospital, he worked as pediatrician for several years. From 1972 to 1975, he worked in the embryology and cytogenetics laboratory at the Department of Gynaecology and Obstetrics in the Cantonal Hospital, Geneva University.[4] He was appointed Professor and Chairman of the Department of Human Genetics at Nagasaki University in 1984.[3] After retiring from the position and becoming Professor Emeritus, he was Professor and Director at Research Institute of Personalized Health Sciences, Health Sciences University of Hokkaido where he became president in 2010.
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论文共 150 篇作者统计合作学者相似作者
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Nobuo Matsuura,Tadashi Kaname,Norio Niikawa,Yoshihide Ooyama, Osamu Shinohara,Yukifumi Yokota,Shigeyuki Ohtsu,Noriyuki Takubo,Kazuteru Kitsuda,Keiko Shibayama,Fumio Takada, Akemi Koike,
semanticscholar(2018)
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Yusuke S Hori, Aiko Yamada, Norifumi Matsuda, Yusuke Ono,Dmytro Starenki,Nadiya Sosonkina,Koh-Ichiro Yoshiura,Norio Niikawa,Tohru Ohta
Yusuke Hori, Aiko Yamada, Norifumi Matsuda, Yusuke Ono,Dmytro Starenki,Nadiya Sosonkina,Koh-ichiro Yoshiura,Norio Niikawa,Tohru Ohta
Human Biologyno. 4 (2017): 305-305
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Frontiers in genetics (2013): 306-306
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