Showing results (41-50 of 81) with videos related to
Sort By:
Pageof 9
Pediatrics|June 3, 2006
Familial and genetic susceptibility to major neonatal morbidities in preterm twinsVineet Bhandari, Matthew J Bizzarro, Anupama Shetty, et al.International Journal of Pediatric Endocrinology|April 25, 2012
Molecular diagnostic testing for Klinefelter syndrome and other male sex chromosome aneuploidiesKarl Hager, Kori Jennings, Seiyu Hosono, et al.Behavior Genetics|November 4, 2010
Pleiotropic effects of DCDC2 and DYX1C1 genes on language and mathematics traits in nuclear families of developmental dyslexiaCecilia Marino, Sara Mascheretti, Valentina Riva, et al.Journal of Autoimmunity|July 30, 2002
Expression, genomic structure and mapping of the thymus specific protease prss16: a candidate gene for insulin dependent diabetes mellitus susceptibilitySaijai Cheunsuk, Rachel Sparks, Janice K Noveroske, et al.American Journal of Human Genetics|June 11, 2013
Alleles of a polymorphic ETV6 binding site in DCDC2 confer risk of reading and language impairmentNatalie R Powers, John D Eicher, Falk Butter, et al.Frontiers in Cell and Developmental Biology|August 26, 2022
Dyslexia associated gene KIAA0319 regulates cell cycle during human neuroepithelial cell developmentSteven Paniagua, Bilal Cakir, Yue Hu, et al.Child Neuropsychology : a Journal on Normal and Abnormal Development in Childhood and Adolescence|August 15, 2019
Effect of READ1 on latent profiles of reading disorder and comorbid attention and language impairment subtypesMiao Li, Dongnhu T Truong, Mellissa DeMille, et al.Plos One|May 22, 2013
Associations of prenatal nicotine exposure and the dopamine related genes ANKK1 and DRD2 to verbal languageJohn D Eicher, Natalie R Powers, Kelly Cho, et al.Behavior Genetics|November 3, 2010
A dyslexia-associated variant in DCDC2 changes gene expressionHaiying Meng, Natalie R Powers, Ling Tang, et al.Human Genetics|September 1, 2005
TDT-association analysis of EKN1 and dyslexia in a Colorado twin cohortHaiying Meng, Karl Hager, Matthew Held, et al.Pageof 9