Author:
Vallianatos Christina N.,Farrehi Clara,Friez Michael J.,Burmeister Margit,Keegan Catherine E.,Iwase Shigeki
Funder
National Institute of General Medical Sciences
National Institute of Child Health and Human Development
National Institute of Neurological Disorders and Stroke
Autism Science Foundation
Michigan Institute for Clinical and Health Research
Horace H. Rackham School of Graduate Studies, University of Michigan
March of Dimes Foundation
Subject
Cellular and Molecular Neuroscience,Molecular Biology
Reference36 articles.
1. Mutations in JARID1C are associated with X-linked mental retardation, short stature and hyperreflexia.;Abidi;J. Med. Genet.,2008
2. A novel mutation in JARID1C/SMCX in a patient with autism spectrum disorder (ASD).;Adegbola;Am. J. Med. Genet. Part A,2008
3. Sequencing of first-strand cDNA library reveals full-length transcriptomes.;Agarwal;Nat. Commun.,2015
4. Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation.;Allen;Am. J. Hum. Genet.,1992
Cited by
57 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献