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Journal of Human Genetics|November 23, 2012
Genotype instability during long-term subculture of lymphoblastoid cell linesJi Hee Oh, Young Jin Kim, Sanghoon Moon, et al.Journal of Human Genetics|May 4, 2012
Genome-wide association studies of tuberculosis in Asians identify distinct at-risk locus for young tuberculosisSurakameth Mahasirimongkol, Hideki Yanai, Taisei Mushiroda, et al.Journal of Human Genetics|May 4, 2012
New mutations in the GLA gene in Brazilian families with Fabry diseaseLauro Thiago Turaça, Juliana Gilbert Pessoa, Fabiana Louise Motta, et al.Journal of Human Genetics|June 1, 2012
A powerful parent-of-origin effects test for qualitative traits incorporating control children in nuclear familiesJi-Yuan Zhou, Wei-Gao Mao, Dan-Ling Li, et al.Journal of Human Genetics|June 1, 2012
Screening of genes involved in chromosome segregation during meiosis I: in vitro gene transfer to mouse fetal oocytesMakiko Tsutsumi, Hiroe Kowa-Sugiyama, Hasbaira Bolor, et al.Journal of Human Genetics|August 9, 2013
Galactosemia in the Turkish population with a high frequency of Q188R mutation and distribution of Duarte-1 and Duarte-2 variationsRıza Köksal Özgül, Ayşegül Güzel-Ozantürk, Halil Dündar, et al.Journal of Human Genetics|August 30, 2013
An Xp22.12 microduplication including RPS6KA3 identified in a family with variably affected intellectual and behavioral disabilitiesAyumi Matsumoto, Mari Kuwajima, Kunio Miyake, et al.Journal of Human Genetics|March 18, 2011
Familial skewed X-chromosome inactivation linked to a component of the cohesin complex, SA2Nisa K E Renault, Marc P Renault, Emily Copeland, et al.Journal of Human Genetics|March 18, 2011
Exploration of the disease locus by a careful evaluation of the likelihood polynomial for pedigree dataYuki Sugaya, Ritei ShibataJournal of Human Genetics|August 5, 2011
p53 Arg72Pro and MDM2 309 SNPs in hereditary retinoblastomaMaria Carmela Epistolato, Vittoria Disciglio, Gabriella Livide, et al.Pageof 351