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Journal of Human Genetics|March 29, 2022
Y-SNP Haplogroup Hierarchy Finder: a web tool for Y-SNP haplogroup assignmentBill Tseng, Hsiao-Lin Hwa, Chun-Yen Lin, et al.Journal of Human Genetics|March 26, 2022
Biallelic BICD2 variant is a novel candidate for Cohen-like syndromeAhmet Okay Caglayan, Beyhan Tuysuz, Ece Gül, et al.Journal of Human Genetics|September 16, 2018
Catechol-O-methyltransferase (COMT) genotypes are associated with varying soluble, but not membrane-bound COMT protein in the human prefrontal cortexGeorgia M Parkin, Madhara Udawela, Andrew Gibbons, et al.Journal of Human Genetics|September 20, 2018
A novel truncating mutation in MYH3 causes spondylocarpotarsal synostosis syndrome with basilar invaginationMasaki Takagi, Satoshi Shimomura, Ryuji Fukuzawa, et al.Journal of Human Genetics|September 7, 2018
A comparison of genome cohort participants' genetic knowledge and preferences to receive genetic results before and after a genetics workshopKayono Yamamoto, Atsushi Shimizu, Fumie Aizawa, et al.Journal of Human Genetics|September 30, 2018
Correction: A novel NDUFS3 mutation in a Chinese patient with severe Leigh syndromeXiaoting Lou, Hao Shi, Shumeng Wen, et al.Journal of Human Genetics|September 13, 2018
Clinical and genetic backgrounds of hypertrophic cardiomyopathy with mid-ventricular obstructionNatsuko Inagaki, Takeharu Hayashi, Yasuyoshi Takei, et al.Journal of Human Genetics|October 11, 2018
PLA2G6-associated neurodegeneration presenting as a complicated form of hereditary spastic paraplegiaKishin Koh, Yuta Ichinose, Hiroyuki Ishiura, et al.Journal of Human Genetics|March 7, 2022
Genome-wide association study identifies APOE locus influencing plasma p-tau181 levelsYu-Yuan Huang, Yu-Xiang Yang, Hui-Fu Wang, et al.Journal of Human Genetics|March 18, 2000
Human C-reactive protein (CRP) 1059G/C polymorphismH Cao, R A HegelePageof 351