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Human Genetics|December 19, 2013
Identification of BACH2 as a susceptibility gene for Graves' disease in the Chinese Han population based on a three-stage genome-wide association studyWei Liu, Hai-Ning Wang, Zhao-Hui Gu, et al.Human Genetics|April 5, 2016
Erratum to: Quantifying the legacy of the Chinese Neolithic on the maternal genetic heritage of Taiwan and Island Southeast AsiaAndreia Brandão, Ken Khong Eng, Teresa Rito, et al.Human Genetics|April 5, 2016
Refining the Y chromosome phylogeny with southern African sequencesChiara Barbieri, Alexander Hübner, Enrico Macholdt, et al.Human Genetics|April 7, 2016
De novo mutations in CSNK2A1 are associated with neurodevelopmental abnormalities and dysmorphic featuresVolkan Okur, Megan T Cho, Lindsay Henderson, et al.Human Genetics|April 13, 2016
Polymorphisms in the MTHFR gene influence embryo viability and the incidence of aneuploidyMaría Enciso, Jonás Sarasa, Leoni Xanthopoulou, et al.Human Genetics|April 24, 2016
An atypical 12q24.31 microdeletion implicates six genes including a histone demethylase KDM2B and a histone methyltransferase SETD1B in syndromic intellectual disabilityJonathan D J Labonne, Kang-Han Lee, Shigeki Iwase, et al.Human Genetics|April 15, 2016
Novel bioinformatic developments for exome sequencingStefan H Lelieveld, Joris A Veltman, Christian GilissenHuman Genetics|April 15, 2016
Assessing the genetic architecture of epithelial ovarian cancer histological subtypesGabriel Cuellar-Partida, Yi Lu, Suzanne C Dixon, et al.Human Genetics|March 1, 1987
Localization and cloning of Xp21 deletion breakpoints involved in muscular dystrophyA P Monaco, C J Bertelson, C Colletti-Feener, et al.Pageof 958