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Journal of Human Genetics|January 16, 2010
Novel deletions causing pseudoxanthoma elasticum underscore the genomic instability of the ABCC6 regionLaura M F Costrop, Olivier O M Vanakker, Lut Van Laer, et al.
Journal of Human Genetics|September 2, 2016
Genetic diversity of two Neolithic populations provides evidence of farming expansions in North ChinaYe Zhang, Jiawei Li, Yongbin Zhao, et al.
Journal of Human Genetics|July 7, 2017
Deep-intronic variant of fukutin is the most prevalent point mutation of Fukuyama congenital muscular dystrophy in JapanKazuhiro Kobayashi, Reiko Kato, Eri Kondo-Iida, et al.
Journal of Human Genetics|September 9, 2016
Effect of migration patterns on maternal genetic structure: a case of Tai-Kadai migration from China to ThailandJatupol Kampuansai, Wibhu Kutanan, Francesca Tassi, et al.
Journal of Human Genetics|August 26, 2016
The microRNA signatures: aberrantly expressed microRNAs in head and neck squamous cell carcinomaKeiichi Koshizuka, Toyoyuki Hanazawa, Ichiro Fukumoto, et al.
Journal of Human Genetics|June 1, 2018
Congenital chloride diarrhea needs to be distinguished from Bartter and Gitelman syndromeNatsuki Matsunoshita, Kandai Nozu, Masahide Yoshikane, et al.
Journal of Human Genetics|June 7, 2018
Association between the FGFR1 rs13317 single nucleotide polymorphism and orbitale-nasion depth based on cephalometric imagesMohamed Adel, Tetsutaro Yamaguchi, Daisuke Tomita, et al.
Journal of Human Genetics|April 20, 2018
No novel, high penetrant gene might remain to be found in Japanese patients with unknown MODYYukio Horikawa, Kazuyoshi Hosomichi, Mayumi Enya, et al.
Journal of Human Genetics|March 14, 2009
William's syndrome: gene expression is related to parental origin and regional coordinate controlJeremy C Collette, Xiao-Ning Chen, Debra L Mills, et al.
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