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Genes|December 23, 2022
Novel Intronic Mutation in VMA21 Causing Severe Phenotype of X-Linked Myopathy with Excessive Autophagy-Case ReportAntoine Pegat, Nathalie Streichenberger, Nicolas Lacoste, et al.
Genes|December 23, 2022
Genotyping by Sequencing (GBS)-Based QTL Mapping for Bacterial Fruit Blotch (BFB) in WatermelonSang-Min Yeo, Jeongeui Hong, Mohammad Rashed Hossain, et al.
Genes|December 23, 2022
Phenotypic Spectrum of NFIA Haploinsufficiency: Two Additional Cases and Review of the LiteratureVeronica Bertini, Francesca Cambi, Alessandro Orsini, et al.
Genes|December 23, 2022
Unraveling Signatures of Local Adaptation among Indigenous Groups from MexicoHumberto García-Ortiz, Francisco Barajas-Olmos, Cecilia Contreras-Cubas, et al.
Genes|December 23, 2022
Whole-Chromosome Karyotyping of Fetal Nucleated Red Blood Cells Using the Ion Proton Sequencing PlatformAngela N Barrett, Zhouwei Huang, Sarah Aung, et al.
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