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Journal of Human Genetics|June 27, 2009
Germline PTCH1 mutations in Japanese basal cell nevus syndrome patientsChiaki Takahashi, Nozomi Kanazawa, Yoshie Yoshikawa, et al.Journal of Human Genetics|July 11, 2009
FGFR2 is associated with hair thickness in Asian populationsAkihiro Fujimoto, Nao Nishida, Ryosuke Kimura, et al.Journal of Human Genetics|August 22, 2009
Association between polymorphisms in glutathione S-transferase Mu3 and IgG titer levels in serum against Helicobacter pyloriMasayuki Tatemichi, Motoki Iwasaki, Shizuka Sasazuki, et al.Journal of Human Genetics|August 22, 2009
Association study of genetic polymorphism in ABCC4 with cyclophosphamide-induced adverse drug reactions in breast cancer patientsSiew-Kee Low, Kazuma Kiyotani, Taisei Mushiroda, et al.Journal of Human Genetics|August 22, 2009
Clinical and genetic investigation of isolated microspherophakia in a consanguineous Tunisian familySalim Ben Yahia, Farah Ouechtati, Bechir Jelliti, et al.Journal of Human Genetics|July 25, 2009
Parent-of-origin of HLA-DRB1*1501 and age of onset of multiple sclerosisSreeram V Ramagopalan, Jake K Byrnes, David A Dyment, et al.Journal of Human Genetics|February 7, 2009
The genetic bases for non-syndromic hearing loss among ChineseXiao Mei Ouyang, Denise Yan, Hui Jun Yuan, et al.Journal of Human Genetics|February 7, 2009
A practical case-control association test for detecting a susceptibility allele at a copy number variation locusJun OhashiJournal of Human Genetics|April 4, 2009
Association of LOXL1 gene with Finnish exfoliation syndrome patientsSusanna Lemmelä, Eva Forsman, Päivi Onkamo, et al.Journal of Human Genetics|April 18, 2009
MEFV mutation carriage in Israeli Jewish individuals from ethnicities with low risk for familial Mediterranean feverOlga Feld, Avi Livneh, Yael Shinar, et al.Pageof 351