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Journal of Genetic Counseling|January 17, 2022
Evolving approaches to prenatal genetic counseling for Spinal Muscular Atrophy in the new treatment eraBethany Zettler, Elicia Estrella, Khalida Liaquat, et al.Journal of Genetic Counseling|October 4, 2014
"Is it going to hurt?": the impact of the diagnostic odyssey on children and their familiesNikkola Carmichael, Judith Tsipis, Gail Windmueller, et al.American Journal of Medical Genetics. Part A|August 17, 2022
Upper motor neuron signs and early onset gait abnormalities in young children with bi-allelic VWA1 variantsDustin L Gable, Alisa Mo, Elicia Estrella, et al.Journal of Cardiac Failure|March 9, 2010
Familial dilated cardiomyopathy secondary to dystrophin splice site mutationDita Obler, Bai-Lin Wu, Va Lip, et al.BMC Musculoskeletal Disorders|November 27, 2007
LGMD2I in a North American populationPeter B Kang, Chris A Feener, Elicia Estrella, et al.Cell Stem Cell|September 20, 2016
CD82 Is a Marker for Prospective Isolation of Human Muscle Satellite Cells and Is Linked to Muscular DystrophiesMatthew S Alexander, Anete Rozkalne, Alessandro Colletta, et al.Circulation|June 9, 2004
Recurrent third-trimester fetal loss and maternal mosaicism for long-QT syndromeTodd E Miller, Elicia Estrella, Robert J Myerburg, et al.Pediatric Neurology|June 13, 2009
Congenital myasthenic syndrome with episodic apneaLeah A Mallory, James G Shaw, Stephanie L Burgess, et al.Neurology. Genetics|May 2, 2019
Homozygous TRPV4 mutation causes congenital distal spinal muscular atrophy and arthrogryposisJose Velilla, Michael Mario Marchetti, Agnes Toth-Petroczy, et al.Muscle & Nerve|March 3, 2016
Homozygous nonsense mutation in SGCA is a common cause of limb-girdle muscular dystrophy in Assiut, EgyptHemakumar M Reddy, Sherifa A Hamed, Monkol Lek, et al.Pageof 3