Bridging cognition, the brain and molecular genetics: evidence from Williams syndrome

This publication has 40 references indexed in Scilit:

• Williams Syndrome: Use of Chromosomal Microdeletions as a Tool to Dissect Cognitive and Physical Phenotypes
  American Journal of Human Genetics, 1999
• A Novel Human GeneFKBP6Is Deleted in Williams Syndrome
  Genomics, 1998
• PMS2-Related Genes Flank the Rearrangement Breakpoints Associated with Williams Syndrome and Other Diseases on Human Chromosome 7
  Genomics, 1997
• Word learning in a special population: do individuals with Williams syndrome obey lexical constraints?
  Journal of Child Language, 1997
• Hemizygous Deletion of the Syntaxin 1A Gene in Individuals with Williams Syndrome
  American Journal of Human Genetics, 1997
• Contrasting profiles of language development in children with williams and down syndromes
  Developmental Neuropsychology, 1997
• Delineation of 7q11.2 Deletions Associated with Williams–Beuren Syndrome and Mapping of a Repetitive Sequence to within and to Either Side of the Common Deletion
  Genomics, 1996
• Unique Profile of Visuo-Perceptual Skills in a Genetic Syndrome
  Brain and Cognition, 1995
• Cytoarchitectonic anomalies in a genetically based disorder
  NeuroReport, 1994
• A SURVEY OF ADULTS WITH WILLIAMS SYNDROME AND IDIOPATHIC INFANTILE HYPERCALCAEMIA
  Developmental Medicine and Child Neurology, 1990