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

Podobne zapisy

• The Common Inversion of the Williams–Beuren Syndrome Region at 7q11.23 Does Not Cause Clinical Symptoms
  od: Tam, Elaine, i wsp.
  Wydane: (2008)
• Rearrangements of the Williams–Beuren syndrome locus: molecular basis and implications for speech and language development
  od: Osborne, Lucy R., i wsp.
  Wydane: (2007)
• Observation of a parental inversion variant in a rare Williams–Beuren syndrome family with two affected children
  od: Scherer, Stephen W., i wsp.
  Wydane: (2005)
• Prenatal phenotype of Williams–Beuren syndrome and of the reciprocal duplication syndrome
  od: Marcato, Livia, i wsp.
  Wydane: (2014)
• A 1.5 million–base pair inversion polymorphism in families with Williams-Beuren syndrome
  od: Osborne, Lucy R., i wsp.
  Wydane: (2001)