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Human Mutation|January 15, 2004
Mutations of ARX are associated with striking pleiotropy and consistent genotype-phenotype correlationMitsuhiro Kato, Soma Das, Kristin Petras, et al.
NPJ Precision Oncology|July 14, 2020
Integrated multiomics analysis of hepatoblastoma unravels its heterogeneity and provides novel druggable targetsMasahiro Sekiguchi, Masafumi Seki, Tomoko Kawai, et al.
The Pediatric Infectious Disease Journal|July 30, 2024
Clinical Practice Guidelines for the Management of Congenital Cytomegalovirus Infection in Japan 2023: Executive SummaryYoshinori Ito, Ichiro Morioka, Naoto Takahashi, et al.
Human Molecular Genetics|July 8, 2005
Whole genome association study of rheumatoid arthritis using 27 039 microsatellitesGen Tamiya, Minori Shinya, Tadashi Imanishi, et al.
Nature Genetics|July 4, 2017
Recurrent SPI1 (PU.1) fusions in high-risk pediatric T cell acute lymphoblastic leukemiaMasafumi Seki, Shunsuke Kimura, Tomoya Isobe, et al.
Annals of the Rheumatic Diseases|March 19, 2017
Transethnic meta-analysis identifies GSDMA and PRDM1 as susceptibility genes to systemic sclerosisChikashi Terao, Takahisa Kawaguchi, Philippe Dieude, et al.
The Journal of Investigative Dermatology|November 26, 2010
Meta-analysis confirms the LCE3C_LCE3B deletion as a risk factor for psoriasis in several ethnic groups and finds interaction with HLA-Cw6Eva Riveira-Munoz, Su-Min He, Georgia Escaramís, et al.
Nature Communications|January 31, 2024
GWAS for systemic sclerosis identifies six novel susceptibility loci including one in the Fcγ receptor regionYuki Ishikawa, Nao Tanaka, Yoshihide Asano, et al.
Science (New York, N.Y.)|December 17, 2009
Mapping human genetic diversity in Asia, Mahmood Ameen Abdulla, Ikhlak Ahmed, et al.
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