Severe Expressive-Language Delay Related to Duplication of the Williams–Beuren Locus

Antzeko izenburuak

• Rearrangements of the Williams–Beuren syndrome locus: molecular basis and implications for speech and language development
  nork: Osborne, Lucy R., et al.
  Argitaratua: (2007)
• The Common Inversion of the Williams–Beuren Syndrome Region at 7q11.23 Does Not Cause Clinical Symptoms
  nork: Tam, Elaine, et al.
  Argitaratua: (2008)
• Observation of a parental inversion variant in a rare Williams–Beuren syndrome family with two affected children
  nork: Scherer, Stephen W., et al.
  Argitaratua: (2005)
• Prenatal phenotype of Williams–Beuren syndrome and of the reciprocal duplication syndrome
  nork: Marcato, Livia, et al.
  Argitaratua: (2014)
• Frequency of the 7q11.23 inversion polymorphism in transmitting parents of children with Williams syndrome and in the general population does not differ between North America and Europe
  nork: Mervis Carolyn B, et al.
  Argitaratua: (2011-02-01)