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Human Genetics|August 19, 2018
Correction to: Canada: will privacy rules continue to favour open science?Adrian ThorogoodHuman Genetics|July 15, 2018
Integrated analysis of human genetic association study and mouse transcriptome suggests LBH and SHF genes as novel susceptible genes for amyloid-β accumulation in Alzheimer's diseaseYumi Yamaguchi-Kabata, Takashi Morihara, Tomoyuki Ohara, et al.Human Genetics|July 18, 2018
China: concurring regulation of cross-border genomic data sharing for statist control and individual protectionYongxi Chen, Lingqiao SongHuman Genetics|July 12, 1978
15/17 translocation in acute promyelocytic leukaemiaJ M Scheres, T W Hustinx, G A de Vaan, et al.Human Genetics|March 1, 1991
Gene deletions causing human genetic disease: mechanisms of mutagenesis and the role of the local DNA sequence environmentM Krawczak, D N CooperHuman Genetics|March 1, 1991
The human placental protein 14 (PP14) gene is localized on chromosome 9q34N Van Cong, C Vaisse, M S Gross, et al.Human Genetics|March 1, 1991
Duplications of the X chromosome in males: evidence that most parts of the X chromosome can be active in two copiesM Schmidt, D Du Sart, P Kalitsis, et al.Human Genetics|April 27, 2017
A rare variant in the FHL1 gene associated with X-linked recessive hypoparathyroidismNir Pillar, Oren Pleniceanu, Mingyan Fang, et al.Human Genetics|June 11, 2017
The landscape of genetic diseases in Saudi Arabia based on the first 1000 diagnostic panels and exomesDorota Monies, Mohamed Abouelhoda, Moeenaldeen AlSayed, et al.Human Genetics|October 23, 2009
Genetic variants in the RELN gene are associated with otosclerosis in multiple European populationsIsabelle Schrauwen, Megan Ealy, Erik Fransen, et al.Pageof 958