Deletions and epimutations affecting the human 14q32.2 imprinted region in individuals with paternal and maternal upd(14)-like phenotypes
Masayo Kagami(National Center For Child Health and Development), Tsutomu Ogata(Hamamatsu University School of Medicine), Hirofumi Ohashi(Aichi Medical University), Hiroshi Kishimoto(Tokyo Medical and Dental University), Fumiko Kato(National Center For Child Health and Development), Gen Nishimura(Musashino University), Kenji Kurosawa(Kanagawa Children's Medical Center), Kenjirou Kosaki(Pediatrics and Genetics), Yukichi Tanaka, Shunji Yamamori(Mitsubishi Group (Japan)), Hiroko Kouzan(Takamatsu Red Cross Hospital), Yoichi Sekita(Tokyo Medical and Dental University), Yoko Tanaka(Tokyo Dental College Ichikawa General Hospital), Fumitoshi Ishino(National Institute for Land and Infrastructure Management), Anne C. Ferguson‐Smith(University of Cambridge), Kentarou Matsuoka(National Center For Child Health and Development), Mika Noguchi(Chiba Kaihin Municipal Hospital), Kouji Masumoto(Kyushu University), Tsutomu Takahashi(National Center of Neurology and Psychiatry), Yumiko Komatsu(Kyoto University), Masahiro Nakayama(Osaka International Cancer Institute), Michiyo Okada, Masahito Irie(Tokyo Medical and Dental University)
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