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Journal of Human Genetics|June 11, 1998
Retrotransposal integration of mobile genetic elements in human diseasesY MikiJournal of Human Genetics|June 11, 1998
Mutational analysis of the RET proto-oncogene in 71 Japanese patients with medullary thyroid carcinomaS Shirahama, K Ogura, H Takami, et al.Journal of Human Genetics|June 11, 1998
Mutations in the hepatocyte nuclear factor-1 alpha gene (MODY3) are not a major cause of early-onset non-insulin-dependent (type 2) diabetes mellitus in JapaneseH Nishigori, S Yamada, T Kohama, et al.Journal of Human Genetics|June 11, 1998
Analysis of bilirubin uridine 5'-diphosphate (UDP)-glucuronosyltransferase gene mutations in seven patients with Crigler-Najjar syndrome type IIK Yamamoto, Y Soeda, T Kamisako, et al.Journal of Human Genetics|June 11, 1998
Cloning and chromosomal mapping of a novel ABC transporter gene (hABC7), a candidate for X-linked sideroblastic anemia with spinocerebellar ataxiaY Shimada, S Okuno, A Kawai, et al.Journal of Human Genetics|June 11, 1998
Genomic organization and mapping of the human activin receptor type IIB (hActR-IIB) geneS Ishikawa, M Kai, Y Murata, et al.Journal of Human Genetics|June 11, 1998
A polymorphic CA repeat sequence at the human calcitonin locusK Tsukamoto, M EmiJournal of Human Genetics|May 22, 2015
GWA meta-analysis of personality in Korean cohortsBo-Hye Kim, Han-Na Kim, Seung-Ju Roh, et al.Journal of Human Genetics|May 22, 2015
Brachydactyly Type C patient with compound heterozygosity for p.Gly319Val and p.Ile358Thr variants in the GDF5 proregion: benign variants or mutations?Katja Stange, Claus-Eric Ott, Mareen Schmidt-von Kegler, et al.Journal of Human Genetics|May 22, 2015
Genetics of atrial fibrillation: from families to genomesIngrid E Christophersen, Patrick T EllinorPageof 353