Williams syndrome: use of chromosomal microdeletions as a tool to dissect cognitive and physical phenotypes.

Lignende værker

• Using case study comparisons to explore genotype-phenotype correlations in Williams-Beuren syndrome
  af: Karmiloff-Smith, A, et al.
  Udgivet: (2003)
• Social Cognition in Williams Syndrome: Genotype/Phenotype Insights from Partial Deletion Patients
  af: Karmiloff-Smith, Annette, et al.
  Udgivet: (2012)
• Y chromosome microdeletions in infertile men: prevalence, phenotypes and screening markers for the Indian population
  af: Sen, S., et al.
  Udgivet: (2013)
• Differing Microdeletion Sizes and Breakpoints in Chromosome 7q11.23 in Williams-Beuren Syndrome Detected by Chromosomal Microarray Analysis
  af: Li, Lin, et al.
  Udgivet: (2016)
• Williams-Beuren syndrome: phenotypic variability and deletions of chromosomes 7, 11, and 22 in a series of 52 patients.
  af: Joyce, C A, et al.
  Udgivet: (1996)