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Human Genetics|April 7, 2010
Evidence for inheritance in patients with VACTERL associationBenjamin D Solomon, Daniel E Pineda-Alvarez, Manu S Raam, et al.American Journal of Human Genetics|August 20, 2020
The Role of Host Genetic Factors in Coronavirus Susceptibility: Review of Animal and Systematic Review of Human LiteratureMarissa LoPresti, David B Beck, Priya Duggal, et al.Developmental Medicine and Child Neurology|November 21, 2012
Symptomatology of autism spectrum disorder in a population with neurofibromatosis type 1Karin S Walsh, Jorge I Vélez, Peter G Kardel, et al.American Journal of Medical Genetics. Part A|August 29, 2018
Phenotypic diversity of patients diagnosed with VACTERL associationMajid Husain, Marina Dutra-Clarke, Bryan Lemieux, et al.American Journal of Medical Genetics. Part A|September 17, 2008
Agenesis and dysgenesis of the corpus callosum: clinical, genetic and neuroimaging findings in a series of 41 patientsChayim Can Schell-Apacik, Kristina Wagner, Moritz Bihler, et al.Human Genetics|June 20, 2002
A loss-of-function mutation in the CFC domain of TDGF1 is associated with human forebrain defectsJune M de la Cruz, Richard N Bamford, Rebecca D Burdine, et al.Biological Psychiatry|October 4, 2016
An Ultraconserved Brain-Specific Enhancer Within ADGRL3 (LPHN3) Underpins Attention-Deficit/Hyperactivity Disorder SusceptibilityAriel F Martinez, Yu Abe, Sungkook Hong, et al.Human Molecular Genetics|September 16, 2008
Mutations in the human SIX3 gene in holoprosencephaly are loss of functionSabina Domené, Erich Roessler, Kenia B El-Jaick, et al.Omics : a Journal of Integrative Biology|May 16, 2018
Genomics and Epigenomics of Congenital Heart Defects: Expert Review and Lessons Learned in AfricaNicholas Ekow Thomford, Kevin Dzobo, Nana Akyaa Yao, et al.Elife|January 16, 2014
T cell immunodominance is dictated by the positively selecting self-peptideWan-Lin Lo, Benjamin D Solomon, David L Donermeyer, et al.Pageof 29