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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. 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 ...
  8. ELN-Related Cutis Laxa - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK584550
    ... assessed in the paternal grandparents of the proband. Williams syndrome (WS) is an autosomal dominant disorder characterized by ... of Williams-Beuren syndrome. 7q11.23 duplication syndrome (Williams syndrome region duplication syndrome) is caused by duplication of ...
  9. Noonan Syndrome with Multiple Lentigines - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK1383
    ... lentigines (NSML) should be distinguished from Turner syndrome, Williams syndrome, and monogenic disorders with developmental delay, short stature, ... and left-sided heart defects are the rule. Williams syndrome and NSML are relatively distinct, as they are ...
  10. Developmental Disabilities 
    https://medlineplus.gov/developmentaldisabilities.html
    Developmental disabilities can be physical, mental, or both. The problems are usually life-long, but therapy can help. Learn more. ... What are developmental ...
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