Showing results (4541-4550 of 7,440) with videos related to
Sort By:
Pageof 744
Nature Genetics|June 30, 2015
The support of human genetic evidence for approved drug indicationsMatthew R Nelson, Hannah Tipney, Jeffery L Painter, et al.Nature Genetics|May 26, 2015
Inactivating mutations in MFSD2A, required for omega-3 fatty acid transport in brain, cause a lethal microcephaly syndromeAlicia Guemez-Gamboa, Long N Nguyen, Hongbo Yang, et al.Nature Genetics|May 26, 2015
A cascade of arabinosyltransferases controls shoot meristem size in tomatoCao Xu, Katie L Liberatore, Cora A MacAlister, et al.Nature Genetics|June 2, 2015
Construction of a population-specific HLA imputation reference panel and its application to Graves' disease risk in JapaneseYukinori Okada, Yukihide Momozawa, Kyota Ashikawa, et al.Nature Genetics|June 2, 2015
Mutations in the unfolded protein response regulator ATF6 cause the cone dysfunction disorder achromatopsiaSusanne Kohl, Ditta Zobor, Wei-Chieh Chiang, et al.Nature Genetics|June 2, 2015
Common variants at 10p12.31, 10q21.1 and 13q12.13 are associated with sporadic pituitary adenomaZhao Ye, Zhiqiang Li, Yongfei Wang, et al.Nature Genetics|June 2, 2015
An allelic series of miR-17 ∼ 92-mutant mice uncovers functional specialization and cooperation among members of a microRNA polycistronYoon-Chi Han, Joana A Vidigal, Ping Mu, et al.Nature Genetics|November 5, 1997
A novel gene encoding an SH3 domain protein is mutated in nephronophthisis type 1F Hildebrandt, E Otto, C Rensing, et al.Nature Genetics|November 5, 1997
Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type IIID B Simon, R S Bindra, T A Mansfield, et al.Nature Genetics|November 5, 1997
Identification of PAHX, a Refsum disease geneS J Mihalik, J C Morrell, D Kim, et al.Pageof 744