Showing results (1571-1580 of 3,522) with videos related to
Sort By:
Pageof 353
Journal of Human Genetics|April 1, 2016
New native South American Y chromosome lineagesMarilza S Jota, Daniela R Lacerda, José R Sandoval, et al.Journal of Human Genetics|April 1, 2016
WDR45 mutations in three male patients with West syndromeMitsuko Nakashima, Kyoko Takano, Yu Tsuyusaki, et al.Journal of Human Genetics|April 1, 2016
Exome sequencing reveals two novel compound heterozygous XYLT1 mutations in a Polish patient with Desbuquois dysplasia type 2 and growth hormone deficiencyAleksander Jamsheer, Ewelina M Olech, Kazimierz Kozłowski, et al.Journal of Human Genetics|April 22, 2016
KIAA0319 gene polymorphisms are associated with developmental dyslexia in Chinese Uyghur childrenHua Zhao, Yun Chen, Bao-Ping Zhang, et al.Journal of Human Genetics|July 28, 2017
Postmortem genetic analysis of sudden unexpected death in infancy: neonatal genetic screening may enable the prevention of sudden infant deathYuki Oshima, Takuma Yamamoto, Taisuke Ishikawa, et al.Journal of Human Genetics|October 26, 2017
2SNP heritability and effects of genetic variants for neutrophil-to-lymphocyte and platelet-to-lymphocyte ratioBochao Danae Lin, Elena Carnero-Montoro, Jordana T Bell, et al.Journal of Human Genetics|August 25, 2017
Shared genetic variants for polypoidal choroidal vasculopathy and typical neovascular age-related macular degeneration in East AsiansQiao Fan, Chui Ming Gemmy Cheung, Li Jia Chen, et al.Journal of Human Genetics|September 8, 2017
The clinical characteristics of Asian patients with classical-type Hutchinson-Gilford progeria syndromeNanae Sato-Kawano, Minoru Takemoto, Emiko Okabe, et al.Journal of Human Genetics|July 14, 2017
Genetic variants underlying vitamin D metabolism and VDR-TGFβ-1-SMAD3 interaction may impact on HCV progression: a study based on dbGaP data from the HALT-C studyLaura A de Azevedo, Ursula Matte, Themis R da Silveira, et al.Journal of Human Genetics|March 4, 2016
Clinical manifestations and growth of patients with urea cycle disorders in JapanKimitoshi Nakamura, Jun Kido, Shirou Matsumoto, et al.Pageof 353