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Plos Genetics|December 27, 2018
Correction: Loss of the BMP Antagonist, SMOC-1, Causes Ophthalmo-Acromelic (Waardenburg Anophthalmia) Syndrome in Humans and MiceJoe Rainger, Ellen van Beusekom, Jacqueline K Ramsay, et al.Human Molecular Genetics|August 3, 2013
A comprehensive molecular study on Coffin-Siris and Nicolaides-Baraitser syndromes identifies a broad molecular and clinical spectrum converging on altered chromatin remodelingDagmar Wieczorek, Nina Bögershausen, Filippo Beleggia, et al.Neuron|November 6, 2015
Genes that Affect Brain Structure and Function Identified by Rare Variant Analyses of Mendelian Neurologic DiseaseEnder Karaca, Tamar Harel, Davut Pehlivan, et al.Frontiers in Pediatrics|May 31, 2021
Epidemiological, Clinical, and Laboratory Features of Children With COVID-19 in TurkeyAdem Karbuz, Gulsen Akkoc, Tugba Bedir Demirdag, et al.Functional & Integrative Genomics|January 31, 2022
Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics ConsortiumMunis Dundar, Umut Fahrioglu, Saliha Handan Yildiz, et al.Pageof 15