Clinical utility gene card for: Williams–Beuren Syndrome [7q11.23]

Ítems similars

• Detection of deletions at 7q11.23 in Williams-Beuren syndrome by polymorphic markers
  per: Dutra, Roberta Lelis, et al.
  Publicat: (2011)
• An atypical 7q11.23 deletion in a normal IQ Williams–Beuren syndrome patient
  per: Ferrero, Giovanni Battista, et al.
  Publicat: (2010)
• Reciprocal duplication of the Williams-Beuren syndrome deletion on chromosome 7q11.23 is associated with schizophrenia
  per: Mulle, Jennifer Gladys, et al.
  Publicat: (2013)
• The Common Inversion of the Williams–Beuren Syndrome Region at 7q11.23 Does Not Cause Clinical Symptoms
  per: Tam, Elaine, et al.
  Publicat: (2008)
• Evolutionary mechanisms shaping the genomic structure of the Williams-Beuren syndrome chromosomal region at human 7q11.23
  per: Antonell, Anna, et al.
  Publicat: (2005)