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Journal of Child Neurology|May 22, 2010
Trisomy 8 mosaicism and favorable outcome after treatment of infantile spasms: case reportAnita Datta, Jonathan Picker, Alexander RotenbergJournal of Perinatology : Official Journal of the California Perinatal Association|August 5, 2018
Peri-mortem evaluation of infants who die without a diagnosis: focus on advances in genomic technologyMonica H Wojcik, Dara Brodsky, Jane E Stewart, et al.European Journal of Human Genetics : EJHG|January 31, 2008
Familial deletion within NLGN4 associated with autism and Tourette syndromeAmy Lawson-Yuen, Juan-Sebastian Saldivar, Steve Sommer, et al.Birth Defects Research. Part A, Clinical and Molecular Teratology|June 21, 2005
Smith-Lemli-Opitz syndrome in trisomy 13: how does the mix work?Fowzan S Alkuraya, Jonathan Picker, Mira B Irons, et al.Pediatrics|November 3, 2010
Delayed puberty due to a novel mutation in CHD7 causing CHARGE syndromeAndrew Dauber, Joel N Hirschhorn, Jonathan Picker, et al.Pediatrics|April 4, 2018
HLA-A*31:01 and Oxcarbazepine-Induced DRESS in a Patient With Seizures and Complete DCX DeletionHyun Kim, Laura Chadwick, Yasir Alzaidi, et al.HGG Advances|March 15, 2021
Disruption of CTNND2, encoding delta-catenin, causes a penetrant attention deficit disorder and myopiaAbidemi Adegbola, Richard Lutz, Elina Nikkola, et al.International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|July 13, 2014
EEG abnormalities and seizures in genetically diagnosed Fragile X syndromeTakijah T Heard, Sriram Ramgopal, Jonathan Picker, et al.Frontiers in Bioengineering and Biotechnology|April 4, 2022
Prokaryotic Collagen-Like Proteins as Novel BiomaterialsJonathan Picker, Ziyang Lan, Srishtee Arora, et al.BMC Medical Genetics|July 3, 2013
Compound heterozygosity of predicted loss-of-function DES variants in a family with recessive desminopathyHeather M McLaughlin, Melissa A Kelly, Pamela P Hawley, et al.Pageof 4