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Current Opinion in Neurobiology, ISSN 0959-4388, 06/2013, Volume 23, Issue 3, pp. 414 - 422
Williams syndrome (WS) offers an exciting model for social neuroscience because its genetic basis is well-defined, and the unique phenotype reflects dimensions... 
Amygdala
Journal Article
Hippocampus, ISSN 1050-9631, 03/2014, Volume 24, Issue 3, pp. 354 - 362
Journal Article
Current Opinion in Neurobiology, ISSN 0959-4388, 2013, Volume 23, Issue 3, pp. 414 - 422
Journal Article
Nature, ISSN 0028-0836, 08/2016, Volume 536, Issue 7616, pp. 338 - 343
Journal Article
Journal Article
PLoS Genetics, ISSN 1553-7390, 11/2011, Volume 7, Issue 11
  A significant current challenge in human genetics is the identification of interacting genetic loci mediating complex polygenic disorders. One of the best... 
Heart | Neurosciences | Insects | Microscopy | Rodents | Mortality | Genetics | Gene loci | Chromosomes | Defects
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 7/2009, Volume 106, Issue 29, pp. 12031 - 12036
Journal Article
Development and Psychopathology, ISSN 0954-5794, 12/2008, Volume 20, Issue 1, pp. 1 - 35
Research into phenotype-genotype correlations in neurodevelopmental disorders has greatly elucidated the contribution of genetic and neurobiological factors to... 
MULTIPLE-LEVELS | SUPRAVALVULAR AORTIC STENOSIS | BEUREN-SYNDROME | MENTAL-RETARDATION | COGNITIVE NEUROSCIENCE | LANGUAGE IMPAIRMENT | DOWNS-SYNDROME | PSYCHOLOGY, DEVELOPMENTAL | CORPUS-CALLOSUM | NEURAL BASIS | DEVELOPMENTAL DISORDERS | Williams Syndrome - genetics | Humans | Child, Preschool | Infant | Male | Social Environment | Brain - abnormalities | Williams Syndrome - psychology | Intellectual Disability - genetics | Williams Syndrome - physiopathology | Adult | Female | Child | Cognition Disorders - psychology | Chromosome Deletion | Emotions - physiology | Cognition Disorders - physiopathology | Personality Development | Brain - physiopathology | Genotype | Chromosome Mapping | Cognition Disorders - genetics | Intellectual Disability - physiopathology | Magnetic Resonance Imaging | Phenotype | Cross-Cultural Comparison | Elastin - genetics | Personal Construct Theory | Adolescent | Intellectual Disability - psychology | Chromosomes, Human, Pair 7 - genetics | Neurosciences | Neurobiology | Cognitive ability | Cognition | Gene deletion | Neurodevelopmental disorders | Genotype & phenotype | Functional anatomy | Clonal deletion | Genetics | Behavior | Neuropsychology | Psychopathology | Medical research | Genetic disorders | Chromosome 7 | Chromosome deletion | Gene expression | Williams syndrome | Studies | Brain research | Researchers | Cognition & reasoning | Anxieties | Structure-function relationships | Psychology | Cognitive science | Social behavior | phenotype correlations | Multiple levels of analysis
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 07/2011, Volume 155, Issue 7, pp. 1509 - 1510
Journal Article
PLoS ONE, ISSN 1932-6203, 08/2014, Volume 9, Issue 8, p. e104088
Journal Article