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Journal of Human Genetics|June 18, 2010
Combined effect of longevity-associated mitochondrial DNA 5178 C/A polymorphism and coffee consumption on the risk of hyper-LDL cholesterolemia in middle-aged Japanese menAkatsuki Kokaze, Mamoru Ishikawa, Naomi Matsunaga, et al.Journal of Human Genetics|May 2, 2009
Molecular cloning of t(2;7)(p24.3;p14.2), a novel chromosomal translocation in myelodysplastic syndrome-derived acute myeloid leukemiaKazuhiro Fujita, Masashi Sanada, Hiroshi Harada, et al.Journal of Human Genetics|May 28, 2010
The association of glutathione-S-transferase gene polymorphisms (GSTM1, GSTT1, GSTP1) with idiopathic male infertilityMohammad Reza Safarinejad, Nayyer Shafiei, Shiva SafarinejadJournal of Human Genetics|September 7, 2006
A locus for familial skewed X chromosome inactivation maps to chromosome Xq25 in a family with a female manifesting Lowe syndromeMilena Cau, Maria Addis, Rita Congiu, et al.Journal of Human Genetics|September 15, 2006
Prediction of systemic exposure to cyclosporine in Japanese pediatric patientsToshiyuki Sakaeda, Kazumoto Iijima, Kandai Nozu, et al.Journal of Human Genetics|September 2, 2006
Beta2-adrenergic receptor polymorphisms are associated with asthma and COPD in adultsMelanie C Matheson, Justine A Ellis, Joan Raven, et al.Journal of Human Genetics|September 2, 2006
A founder mutation for ichthyosis prematurity syndrome restricted to 76 kb by haplotype associationM Melin, J Klar, T Jr Gedde-Dahl, et al.Journal of Human Genetics|September 2, 2006
Novel mutation in the HSN2 gene in a Korean patient with hereditary sensory and autonomic neuropathy type 2Hyun-Jung Cho, Byoung Joon Kim, Yeon-Lim Suh, et al.Journal of Human Genetics|April 12, 2007
Gap junction coding genes and schizophrenia: a genetic association studyBranko Aleksic, Ryoko Ishihara, Nagahide Takahashi, et al.Journal of Human Genetics|May 4, 2007
Mutation of junctophilin type 2 associated with hypertrophic cardiomyopathyYoshihisa Matsushita, Toru Furukawa, Hiroshi Kasanuki, et al.Pageof 353