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

Podobne zapisy

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