Mental Retardation: A Review of the Genetic Causes

This publication has 25 references indexed in Scilit:

• Monogenic causes of X-linked mental retardation
  Nature Reviews Genetics, 2001
• The Epidemiology of Mental Retardation of Unknown Cause
  Pediatrics, 2001
• MECP2 is highly mutated in X-linked mental retardation
  Human Molecular Genetics, 2001
• XLMR genes: update 2000
  European Journal of Human Genetics, 2001
• Familial Mental Retardation Syndrome ATR-16 Due to an Inherited Cryptic Subtelomeric Translocation, t(3;16)(q29;p13.3)
  American Journal of Human Genetics, 2000
• Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
  Nature Genetics, 1999
• In Vitro Reactivation of the FMR1 Gene Involved in Fragile X Syndrome
  Human Molecular Genetics, 1998
• Evaluation of mental retardation: Recommendations of a consensus conference
  American Journal of Medical Genetics, 1997
• Identification of the gene FMR2, associated with FRAXE mental retardation
  Nature Genetics, 1996
• The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation
  Nature Genetics, 1995