Unusual cognitive and behavioural profile in a Williams syndrome patient with atypical 7q11.23 deletion

Samankaltaisia teoksia

• An atypical 7q11.23 deletion in a normal IQ Williams–Beuren syndrome patient
  Tekijä: Ferrero, Giovanni Battista, et al.
  Julkaistu: (2010)
• Detection of deletions at 7q11.23 in Williams-Beuren syndrome by polymorphic markers
  Tekijä: Dutra, Roberta Lelis, et al.
  Julkaistu: (2011)
• A 1.3-Mb 7q11.23 Atypical Deletion Identified in a Cohort of Patients with Williams-Beuren Syndrome
  Tekijä: Delgado, L.M., et al.
  Julkaistu: (2013)
• Reciprocal duplication of the Williams-Beuren syndrome deletion on chromosome 7q11.23 is associated with schizophrenia
  Tekijä: Mulle, Jennifer Gladys, et al.
  Julkaistu: (2013)
• Deletions of the elastin gene at 7q11.23 occur in approximately 90% of patients with Williams syndrome.
  Tekijä: Nickerson, E, et al.
  Julkaistu: (1995)