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Journal of Human Genetics|February 1, 2013
Follow-up study of 22 Chinese children with Alexander disease and analysis of parental origin of de novo GFAP mutationsLili Zang, Jingmin Wang, Yuwu Jiang, et al.
Journal of Human Genetics|February 1, 2013
DRD2 haplotype associated with negative symptoms and sustained attention deficits in Han Chinese with schizophrenia in TaiwanYi-Ling Chien, Hai-Gwo Hwu, Cathy S-J Fann, et al.
Journal of Human Genetics|February 1, 2013
Exome sequencing identifies novel rheumatoid arthritis-susceptible variants in the BTNL2Shigeki Mitsunaga, Kazuyoshi Hosomichi, Yuko Okudaira, et al.
Journal of Human Genetics|February 1, 2013
A microRNA-520 mirSNP at the MMP2 gene influences susceptibility to endometriosis in Chinese womenEing-Mei Tsai, Yung-Song Wang, Chang-Shen Lin, et al.
Journal of Human Genetics|January 11, 2013
Genome-wide association study of serum albumin:globulin ratio in Korean populationsKyung-Won Hong, Hyun-Seok Jin, Daesub Song, et al.
Journal of Human Genetics|December 11, 2012
Genomic characterization of two large Alu-mediated rearrangements of the BRCA1 geneAna Peixoto, Manuela Pinheiro, Lígia Massena, et al.
Journal of Human Genetics|December 14, 2012
Phenotypic variability of CLDN14 mutations causing DFNB29 hearing loss in the Pakistani populationZil-e-Huma Bashir, Noreen Latief, Inna A Belyantseva, et al.
Journal of Human Genetics|January 25, 2013
Association of lipoprotein lipase polymorphism rs2197089 with serum lipid concentrations and LPL gene expressionXingbo Mo, Xuehui Liu, Laiyuan Wang, et al.
Journal of Human Genetics|March 8, 2013
Molecular analysis of the genes causing recessive demyelinating Charcot-Marie-Tooth disease in JapanMakiko Hayashi, Akiko Abe, Tatsufumi Murakami, et al.
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