The genetic landscape of intellectual disability arising from chromosome X

This publication has 97 references indexed in Scilit:

• Solution hybrid selection with ultra-long oligonucleotides for massively parallel targeted sequencing
  Nature Biotechnology, 2009
• Structural variation in Xq28: MECP2 duplications in 1% of patients with unexplained XLMR and in 2% of male patients with severe encephalopathy
  European Journal of Human Genetics, 2008
• X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment
  Nature Genetics, 2008
• Oligosaccharyltransferase-Subunit Mutations in Nonsyndromic Mental Retardation
  American Journal of Human Genetics, 2008
• SLC9A6 Mutations Cause X-Linked Mental Retardation, Microcephaly, Epilepsy, and Ataxia, a Phenotype Mimicking Angelman Syndrome
  American Journal of Human Genetics, 2008
• Submicroscopic Duplications of the Hydroxysteroid Dehydrogenase HSD17B10 and the E3 Ubiquitin Ligase HUWE1 Are Associated with Mental Retardation
  American Journal of Human Genetics, 2008
• Genome-wide in situ exon capture for selective resequencing
  Nature Genetics, 2007
• Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation
  Nature Genetics, 2007
• Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project
  Nature, 2007
• Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism
  Nature Genetics, 2003