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Journal of Human Genetics|December 19, 2014
Mutations in the glucocerebrosidase gene are responsible for Chinese patients with Parkinson's diseaseZhe Yu, Ting Wang, Jun Xu, et al.
Journal of Human Genetics|December 18, 2015
Individual risk alleles of susceptibility to schizophrenia are associated with poor clinical and social outcomesShinji Sakamoto, Manabu Takaki, Yuko Okahisa, et al.
Journal of Human Genetics|March 4, 2016
Enigmatic in vivo GlcNAc-1-phosphotransferase (GNPTG) transcript correction to wild type in two mucolipidosis III gamma siblings homozygous for nonsense mutationsRenata Voltolini Velho, Nataniel Floriano Ludwig, Taciane Alegra, et al.
Journal of Human Genetics|February 26, 2016
Two novel mutations in TMEM38B result in rare autosomal recessive osteogenesis imperfectaFang Lv, Xiao-Jie Xu, Jian-Yi Wang, et al.
Journal of Human Genetics|December 15, 2015
Gene-environment interactions in obesity: implication for future applications in preventive medicineSho Nakamura, Hiroto Narimatsu, Hidenori Sato, et al.
Journal of Human Genetics|December 15, 2015
First independent replication of the involvement of LARS2 in Perrault syndrome by whole-exome sequencing of an Italian familyGiulia Soldà, Sonia Caccia, Michela Robusto, et al.
Journal of Human Genetics|November 29, 2013
The tumor-suppressive microRNA-143/145 cluster inhibits cell migration and invasion by targeting GOLM1 in prostate cancerSatoko Kojima, Hideki Enokida, Hirofumi Yoshino, et al.
Journal of Human Genetics|July 11, 2014
No association between Y chromosomal haplogroups and severe acne in the Han Chinese populationMei-Hua Guo, Wen-Juan Wu, Long Fan, et al.
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