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BMC Medical Genomics|July 21, 2016
Exome sequencing in mostly consanguineous Arab families with neurologic disease provides a high potential molecular diagnosis rateWu-Lin Charng, Ender Karaca, Zeynep Coban Akdemir, et al.Wires Mechanisms of Disease|January 8, 2024
Let's talk about sex: Mechanisms of neural sexual differentiation in BilateriaEmma C Roggenbuck, Elijah A Hall, Isabel B Hanson, et al.The Journal of Clinical Investigation|January 12, 2016
Molecular etiology of arthrogryposis in multiple families of mostly Turkish originYavuz Bayram, Ender Karaca, Zeynep Coban Akdemir, et al.The Journal of Clinical Investigation|January 10, 2015
Global transcriptional disturbances underlie Cornelia de Lange syndrome and related phenotypesBo Yuan, Davut Pehlivan, Ender Karaca, et al.Science (New York, N.Y.)|December 14, 2019
Why whales are big but not bigger: Physiological drivers and ecological limits in the age of ocean giantsJ A Goldbogen, D E Cade, D M Wisniewska, et al.Human Mutation|May 5, 2006
The spectrum of WRN mutations in Werner syndrome patientsShurong Huang, Lin Lee, Nancy B Hanson, 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.Nature Aging|August 10, 2023
Universal DNA methylation age across mammalian tissuesA T Lu, Z Fei, A Haghani, et al.Pageof 28