Cover Image, Volume 38, Issue 3. Issue 3 (March 2017)

• Record Type: Journal Article
• Authors: Takeda, Kazuki; Kou, Ikuyo; Kawakami, Noriaki; Iida, Aritoshi; Nakajima, Masahiro; Ogura, Yoji; Imagawa, Eri; Miyake, Noriko; Matsumoto, Naomichi; Yasuhiko, Yukuto; Sudo, Hideki; Kotani, Toshiaki; Nakamura, Masaya; Matsumoto, Morio; Watanabe, Kota; Ikegawa, Shiro
• Is Part Of: Human mutation. Volume 38:Issue 3(2017)
• Page Start: i
• Page End: i
• Publication Date: 2017-03
• Subjects: Human chromosome abnormalities -- Periodicals; Mutation (Biology) -- Periodicals; 616.04205
• DOI: 10.1002/humu.23194
• Languages: English
• ISSNs: 1059-7794

Abstract

Abstract : On the cover : The image, provided courtesy of Dr. G. Thomas Watters, Ohio State University, is based on the Original article, Compound heterozygosity for null mutations and a common hypomorphic risk haplotype in TBX6 causes congenital scoliosis, by Shiro Ikegawa et al., Pages 317–323. DOI:10.1002/humu.23168 .