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122 results

  1. Cohen Syndrome - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK1482
    ... with Bardet-Biedl syndrome. Inheritance is autosomal recessive. Cri-du-chat syndrome (OMIM 123450 ) is a multiple congenital anomaly syndrome ...
  2. Literature Search Methods - Genetic Testing for Developmental Disabilities, Intellectual Disability, and Autism ... 
    https://www.ncbi.nlm.nih.gov/books/NBK310458
    ... Charcot-Marie-Toothe syndrome Conotruncal anomaly face syndrome Cri du Chat syndrome DiGeorge syndrome Down syndrome Fragile x Fragile-x ... OR ‘wagr syndrome’ OR ‘langer gideon syndrome’ OR ‘cri du chat syndrome’ OR ‘wolf-hirschorn syndrome’ OR ‘jacobsen syndrome’ OR ‘ ...
  3. Developmental Disabilities 
    https://medlineplus.gov/developmentaldisabilities.html
    ... Academy of Pediatrics) Also in Spanish Specifics About Cri du Chat Syndrome (National Human Genome Research Institute) Angelman Syndrome (National ... Costello syndrome: MedlinePlus Genetics (National Library of Medicine) ... (National Library of Medicine) Developmental and ...
  4. pdf2018MeShTreeHierarchy.pdf 
    https://www.nlm.nih.gov/mesh/2018/download/2018MeShTreeHierarchy.pdf
    ... 643...........................................Intellectual Disability C10.597.606.643.180...........................................Cri-du-Chat Syndrome C10.597.606.643.210...........................................De Lange Syndrome ...
  5. Clinical evidence – search strategies - Challenging Behaviour and Learning Disabilities - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK355386
    ... or cerebral palsy/ or coffin-lowry syndrome/ or cri-du-chat syndrome/ or de lange syndrome/ or down syndrome/ or ... lowry syndrome] this term only #23. mesh descriptor: [cri-du-chat syndrome] this term only #24. mesh descriptor: [de lange ...
  6. xmlTopicIndex.xml 
    https://medlineplus.gov/download/TopicIndex.xml
    ... topic><topic ><url >https://medlineplus.gov/genetics/condition/cri-du-chat-syndrome</url><title >Cri-du-chat syndrome</title><other_names ><other_name >5p deletion syndrome</ ...
  7. Primary Ciliary Dyskinesia - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK1122
    ... has isolated retinitis pigmentosa and no respiratory manifestations. Cri-du-chat syndrome (OMIM 123450 ) is caused by a segmental chromosome ... be associated with PCD). PCD co-occurs in cri-du-chat syndrome when a PCD-causing pathogenic variant is detected ...
  8. Excluded Studies - Interventions Targeting Sensory Challenges in Children With Autism Spectrum Disorder—An Update - ... 
    https://www.ncbi.nlm.nih.gov/books/NBK448045
    ... of children with Angelman, Cornelia de Lange and Cri du Chat syndromes. J Intellect Disabil Res. 2011 Apr;55(4): ... phenomenology in Cornelia de Lange, Fragile X, and Cri du Chat syndromes: Results from a 2.5 year follow-up. ...
  9. Excluded Studies - Medical Therapies for Children With Autism Spectrum Disorder—An Update - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK448263
    ... of children with Angelman, Cornelia de Lange and Cri du Chat syndromes. J Intellect Disabil Res. 2011 Apr;55(4): ... phenomenology in Cornelia de Lange, Fragile X, and Cri du Chat syndromes: Results from a 2.5 year follow-up. ...
  10. NLM Digital Collections - Birth defects and developmental disabilities : the search for causes and cures 
    Publication: Washington, DC : Trust for America's Health, July 2005
    resource.nlm.nih.gov/101281311
    ... disabilities, but much more research conditions (such as cri-du-chat syndrome or targeted specifically to early recognition and Prader- ...
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