Whole-exome sequencing confirmation of a novel heterozygous mutation in <i>RUNX1</i> in a pregnant woman with platelet disorderMiyuki Obata, Hirohisa Kurachi, Gen Tamiya et al.|Platelets|2014Cited by 5
A Case of Boomerang Dysplasia with a Novel Causative Mutation in Filamin B: Identification of Typical Imaging Findings on Ultrasonography and 3D-CT ImagingSeiji Tsutsumi, Hirohisa Kurachi, Ayako Maekawa et al.|Fetal Diagnosis and Therapy|2012Cited by 3
ISP-10-7 A novel EBP mutation in X-linked dominant chondrodysplasia punctata(Group 10 Perinatology 2,IS Poster,International Session)Seiji Tsutsumi, Hirohisa Kurachi, Kazuhiro Takahashi et al.|日本産科婦人科學會雜誌|2014Cited by 0