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Biology of Reproduction|September 26, 2014
Transcriptome profiling of granulosa and theca cells during dominant follicle development in the horseF Xavier Donadeu, Somayyeh Fahiminiya, Cristina L Esteves, et al.
Molecular Genetics & Genomic Medicine|October 4, 2019
Exome sequencing study of partial agenesis of the corpus callosum in men with developmental delay, epilepsy, and microcephalyJolyane Meloche, Vanessa Brunet, Pierre-Alexandre Gagnon, et al.
Investigative Ophthalmology & Visual Science|February 14, 2017
The Genetic Causes of Nonsyndromic Congenital Retinal Detachment: A Genetic and Phenotypic Study of Pakistani FamiliesVafa Keser, Ayesha Khan, Sorath Siddiqui, et al.
Journal of Medical Genetics|April 16, 2015
Nonsense mutation in the WDR73 gene is associated with Galloway-Mowat syndromeTawfeg Ben-Omran, Somayyeh Fahiminiya, Natalie Sorfazlian, et al.
American Journal of Medical Genetics. Part A|October 30, 2019
Duplication 2p16 is associated with perisylvian polymicrogyriaDina Amrom, Annapurna Poduri, Jennifer S Goldman, et al.
Iscience|March 18, 2024
Identity and nature of neural stem cells in the adult human subventricular zoneSalma Baig, Javad Nadaf, Redouane Allache, et al.
Clinical Genetics|August 13, 2023
Infantile onset encephalomyopathy, retinopathy, optic atrophy, and mitochondrial DNA depletion associated with a novel pathogenic DHX16 variantMilla-Riikka Hautakangas, Paula Widgren, Paavo Korpelainen, et al.
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