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Annals of Human Genetics|March 1, 2014
Mutation screening of the HGD gene identifies a novel alkaptonuria mutation with significant founder effect and high prevalenceSrinivasan Sakthivel, Andrea Zatkova, Martina Nemethova, et al.
Annals of Human Genetics|February 20, 2002
Angiotensin converting enzyme insertion allele in relation to high altitude adaptationM A Qadar Pasha, A P Khan, R Kumar, et al.
Annals of Human Genetics|July 10, 2023
Uncovering cilia function in glial developmentRachel M Bear, Tamara Caspary
Annals of Human Genetics|July 1, 1983
Quantitative variations in polymorphic types of human red cell esterase DI Nishigaki, T Itoh, N Ogasawara
Annals of Human Genetics|July 7, 2026
Utility of Urine-Derived Cells for Characterizing Aberrant Splicing Caused by a Novel Deep Intronic L1CAM VariantTakuma Harasaki, Sachiko Miyamoto, Takahiro Yonekawa, et al.
Annals of Human Genetics|July 27, 2026
Trans-Ancestry Psychiatric Genomics in Admixed Populations: Advances, Challenges, and Future DirectionsSergio Flores Carrasco, Ángel Roco-Videla, Jorge Briceño-Moya, et al.
Annals of Human Genetics|August 17, 2026
Population-Level Nucleotide Diversity and Genetic Differentiation at SOD1 Across Global Human PopulationsSergio V Flores, Patricia Lillo, Jorge Briceño-Moya
Annals of Human Genetics|August 30, 2026
Decoding the Genetic and Phenotypic Spectrum of MT-TI Mitochondrial DiseasesEnchi Yuan, Ning Zhang, Haoyu He, et al.
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