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A Hodgkinson

Showing results (211-220 of 213) with videos related to

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Human Genetics|October 11, 2021
A pathogenic deletion in Forkhead Box L1 (FOXL1) identifies the first otosclerosis (OTSC) geneNelly Abdelfatah, Ahmed A Mostafa, Curtis R French, et al.
Brain : a Journal of Neurology|November 1, 2016
Genome-wide association study in essential tremor identifies three new lociStefanie H Müller, Simon L Girard, Franziska Hopfner, et al.
Behavior Genetics|September 23, 2015
Association of the OPRM1 Variant rs1799971 (A118G) with Non-Specific Liability to Substance Dependence in a Collaborative de novo Meta-Analysis of European-Ancestry CohortsTae-Hwi Schwantes-An, Juan Zhang, Li-Shiun Chen, et al.
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Showing results (211-220 of 213) with videos related to

Sort By:
Pageof 22
You have reached the last page of results.This site can display upto 213 results.
Human Genetics|October 11, 2021
A pathogenic deletion in Forkhead Box L1 (FOXL1) identifies the first otosclerosis (OTSC) geneNelly Abdelfatah, Ahmed A Mostafa, Curtis R French, et al.
Brain : a Journal of Neurology|November 1, 2016
Genome-wide association study in essential tremor identifies three new lociStefanie H Müller, Simon L Girard, Franziska Hopfner, et al.
Behavior Genetics|September 23, 2015
Association of the OPRM1 Variant rs1799971 (A118G) with Non-Specific Liability to Substance Dependence in a Collaborative de novo Meta-Analysis of European-Ancestry CohortsTae-Hwi Schwantes-An, Juan Zhang, Li-Shiun Chen, et al.
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