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  1. Williams Syndrome - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK1249
    ... Search term GeneReviews Advanced Search Help < Prev Next > Williams Syndrome Synonym: Williams-Beuren Syndrome Colleen A Morris , MD, ... on selection criteria, click here . Canadian Association for Williams Syndrome Canada Phone: 204-256-6594 Email: contact@williamssyndrome. ...
  2. Williams syndrome 
    https://medlineplus.gov/ency/article/001116.htm
    Williams-Beuren syndrome; WBS; Beuren syndrome; 7q11.23 deletion syndrome; Elfin facies syndrome ... Williams syndrome is caused by not having a copy of 25 to 27 genes on chromosome number 7. ...
  3. xmlghr-summaries.xml 
    https://medlineplus.gov/download/ghr-summaries.xml
    ... published></health-condition-summary><health-condition-summary ><name >Williams syndrome</name><ghr-page >https://medlineplus.gov/genetics/condition/ ...
  4. Excluded Studies - Interventions Targeting Sensory Challenges in Children With Autism Spectrum Disorder—An Update - ... 
    https://www.ncbi.nlm.nih.gov/books/NBK448045
    ... S. Social phenotypes of autism spectrum disorders and williams syndrome: similarities and differences. Front Psychol. 2012;3:247. ... in Neurodevelopmental Disorders: The Case of Binding in Williams Syndrome and Autism With and Without Language Impairment. Lang ...
  5. Excluded Studies - Medical Therapies for Children With Autism Spectrum Disorder—An Update - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK448263
    ... S. Social phenotypes of autism spectrum disorders and williams syndrome: similarities and differences. Front Psychol. 2012;3:247. ... in Neurodevelopmental Disorders: The Case of Binding in Williams Syndrome and Autism With and Without Language Impairment. Lang ...
  6. 7q11.23 Duplication Syndrome - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK327268
    ... facial gestalt is not as striking as in Williams syndrome . Neurodevelopment / motor development. Infants with 7q11.23 duplication ... 2009 , Velleman & Mervis 2011 ]. Genetically Related (Allelic) Disorders Williams syndrome (WS) is caused by a recurrent 7q11.23 ...
  7. pdf2017MeshTreesWithChangesShown.pdf 
    https://www.nlm.nih.gov/.../2017MeshTreesWithChangesShown.pdf
    ... Prader-Willi Syndrome Rubinstein-Taybi Syndrome WAGR Syndrome Williams Syndrome Perceptual Disorders Agnosia Gerstmann Syndrome Prosopagnosia Alice in ...
  8. 2019New_Mesh_Tree_Hierarchy.txt 
    https://www.nlm.nih.gov/.../download/2019New_Mesh_Tree_Hierarchy.txt
    ... 969 WAGR Syndrome C10.597.606.360.970 Williams Syndrome C10.597.606.441 Lethargy C10.597.606. ... Stenosis, Supravalvular C14.280.484.150.535.960 Williams Syndrome C14.280.484.400 Heart Valve Prolapse C14. ...
  9. pdf2016MeshTree.pdf 
    https://www.nlm.nih.gov/mesh/2016/download/2016MeshTree.pdf
    ... 969...........................................WAGR Syndrome C10.597.606.643.970...........................................Williams Syndrome Page 312 2016 MeSH Tree Hierarchy Tree location ...
  10. Literature Search Methods - Genetic Testing for Developmental Disabilities, Intellectual Disability, and Autism ... 
    https://www.ncbi.nlm.nih.gov/books/NBK310458
    ... Smith-Magenis SRY deletion Velocardiofacial syndrome Wagr syndrome Williams syndrome Williams-Beuren syndrome Wolf-Hirschorn syndrome Genetic Testing ...
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