Cognitive and Behavioral Characterization of 16p11.2 Deletion Syndrome
作者： Miller DT. Hanson E , Nasir RH , Fong A , Lian A , Hundley R
DOI: 10.1097/DBP.0B013E3181EA50ED
关键词: Autism 、 Language disorder 、 Autism spectrum disorder 、 Bioinformatics 、 Deletion syndrome 、 Communication disorder 、 Psychology 、 Developmental disorder 、 Cognition 、 Pervasive developmental disorder 、 Psychiatry 、 Pediatrics, Perinatology, and Child Health 、 Developmental and Educational Psychology 、 Psychiatry and Mental health
摘要: ABSTRACT:Objective:To describe cognitive and behavioral features of patients with chromosome 16p11.2 deletion syndrome, a recently identified common genetic cause neurodevelopmental disability, especially autism spectrum disorder (ASD).Method:Twenty-one were eva
simonsvipconnect.org 参考文章(30)
Kavita S Reddy, Cytogenetic abnormalities and fragile-x syndrome in Autism Spectrum Disorder BMC Medical Genetics. ,vol. 6, pp. 3- 3 ,(2005) , 10.1186/1471-2350-6-3
Ron Dumont, John O. Willis, Kathleen Veizel, Jamie Zibulsky, Wechsler Abbreviated Scale of Intelligence Encyclopedia of Special Education. ,(2014) , 10.1002/9781118660584.ESE2519
Inge-Marie Eigsti, Peabody Picture Vocabulary Test Corsini Encyclopedia of Psychology. pp. 1- 1 ,(2010) , 10.1002/9780470479216.CORPSY0649
Gurdeep S Sagoo, Adam S Butterworth, Simon Sanderson, Charles Shaw-Smith, Julian P T Higgins, Hilary Burton, Array CGH in patients with learning disability (mental retardation) and congenital anomalies: updated systematic review and meta-analysis of 19 studies and 13,926 subjects Genetics in Medicine. ,vol. 11, pp. 139- 146 ,(2009) , 10.1097/GIM.0B013E318194EE8F
Jami-Jon Mitchell, Comprehensive Test of Phonological Processing Assessment for Effective Intervention. ,vol. 26, pp. 57- 63 ,(2001) , 10.1177/073724770102600305
Nader Ghebranious, Philip F. Giampietro, Frederic P. Wesbrook, Shereif H. Rezkalla, A novel microdeletion at 16p11.2 harbors candidate genes for aortic valve development, seizure disorder, and mild mental retardation† American Journal of Medical Genetics Part A. ,vol. 143, pp. 1462- 1471 ,(2007) , 10.1002/AJMG.A.31837
Jill A. Rosenfeld, Justine Coppinger, Bassem A. Bejjani, Santhosh Girirajan, Evan E. Eichler, Lisa G. Shaffer, Blake C. Ballif, Speech delays and behavioral problems are the predominant features in individuals with developmental delays and 16p11.2 microdeletions and microduplications Journal of Neurodevelopmental Disorders. ,vol. 2, pp. 26- 38 ,(2010) , 10.1007/S11689-009-9037-4
Sharon Bradley-Johnson, Mullen Scales of Early Learning Psychology in the Schools. ,vol. 34, pp. 379- 382 ,(1997) , 10.1002/(SICI)1520-6807(199710)34:4<379::AID-PITS14>3.0.CO;2-E
J. Lipton, M. J. Rivkin, 16p11.2-RELATED PAROXYSMAL KINESIGENIC DYSKINESIA AND DOPA-RESPONSIVE PARKINSONISM IN A CHILD Neurology. ,vol. 73, pp. 479- 480 ,(2009) , 10.1212/WNL.0B013E3181B16393
Nancy J. Mendelsohn, G. Bradley Schaefer, Genetic evaluation of autism. Seminars in Pediatric Neurology. ,vol. 15, pp. 27- 31 ,(2008) , 10.1016/J.SPEN.2008.01.005