The Common Inversion of the Williams–Beuren Syndrome Region at 7q11.23 Does Not Cause Clinical Symptoms

Eitemau Tebyg

• 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
  gan: Mervis Carolyn B, et al.
  Cyhoeddwyd: (2011-02-01)
• 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
  gan: Morris, Colleen A, et al.
  Cyhoeddwyd: (2011)
• Rare and low frequency genomic variants impacting neuronal functions modify the Dup7q11.23 phenotype
  gan: Qaiser, Farah, et al.
  Cyhoeddwyd: (2021)
• Detection of deletions at 7q11.23 in Williams-Beuren syndrome by polymorphic markers
  gan: Dutra, Roberta Lelis, et al.
  Cyhoeddwyd: (2011)
• Clinical utility gene card for: Williams–Beuren Syndrome [7q11.23]
  gan: Koehler, Udo, et al.
  Cyhoeddwyd: (2014)