Bridging cognition, the brain and molecular genetics: evidence from Williams syndrome
- 1 May 1999
- journal article
- review article
- Published by Elsevier BV in Trends in Neurosciences
- Vol. 22 (5), 197-207
- https://doi.org/10.1016/s0166-2236(99)01397-1
Abstract
No abstract availableKeywords
This publication has 39 references indexed in Scilit:
- Williams Syndrome: Use of Chromosomal Microdeletions as a Tool to Dissect Cognitive and Physical PhenotypesAmerican Journal of Human Genetics, 1999
- A Novel Human GeneFKBP6Is Deleted in Williams SyndromeGenomics, 1998
- PMS2-Related Genes Flank the Rearrangement Breakpoints Associated with Williams Syndrome and Other Diseases on Human Chromosome 7Genomics, 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 SyndromeAmerican Journal of Human Genetics, 1997
- Contrasting profiles of language development in children with williams and down syndromesDevelopmental 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 DeletionGenomics, 1996
- Unique Profile of Visuo-Perceptual Skills in a Genetic SyndromeBrain and Cognition, 1995
- Cytoarchitectonic anomalies in a genetically based disorderNeuroReport, 1994
- A SURVEY OF ADULTS WITH WILLIAMS SYNDROME AND IDIOPATHIC INFANTILE HYPERCALCAEMIADevelopmental Medicine and Child Neurology, 1990