Japanese founder duplications/triplications involving BHLHA9 are associated with split-hand/foot malformation with or without long bone deficiency and Gollop-Wolfgang complex
日本创始人发现的涉及BHLHA9基因的重复/三重复与手/足裂畸形（伴或不伴长骨发育不全）和戈洛普-沃尔夫冈综合征相关。
期刊:Orphanet Journal of Rare Diseases
影响因子:3.4
doi:10.1186/s13023-014-0125-5.
Eiko Nagata ,Hiroki Kano ,Fumiko Kato ,Rie Yamaguchi ,Shinichi Nakashima ,Shinichiro Takayama ,Rika Kosaki ,Hidefumi Tonoki ,Seiji Mizuno ,Satoshi Watanabe ,Koh-Ichiro Yoshiura ,Tomoki Kosho ,Tomonobu Hasegawa ,Mamori Kimizuka ,Atsushi Suzuki ,Kenji Shimizu ,Hirofumi Ohashi ,Nobuhiko Haga ,Hironao Numabe ,Emiko Horii ,Toshiro Nagai ,Hiroshi Yoshihashi ,Gen Nishimura ,Tatsushi Toda ,Shuji Takada ,Shigetoshi Yokoyama ,Hiroshi Asahara ,Shinichiro Sano ,Maki Fukami ,Shiro Ikegawa ,Tsutomu Ogata
