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Results 1 - 10 of 52 for Autism 17
  1. Autism spectrum disorder 
    ... review of systematic reviews and meta-analyses. Mol Autism. 2017 Mar 17;8:13. doi: 10.1186/s13229-017-0121-4. eCollection 2017. Citation on PubMed or Free article on PubMed Central Mukherjee SB. Autism Spectrum Disorders - Diagnosis and Management. Indian J Pediatr. ...
    https://medlineplus.gov/genetics/condition/autism-spectrum-disorder - Genetics
  2. CHD8 gene 
    ... of the Chromatin Remodeler CHD8 Define an Emerging Autism Etiology. Front Neurosci. 2015 Dec 17;9:477. doi: 10.3389/fnins.2015.00477. ... EE. Disruptive CHD8 mutations define a subtype of autism early in development. Cell. 2014 Jul 17;158(2):263-276. doi: 10.1016/j. ...
    https://medlineplus.gov/genetics/gene/chd8 - Genetics
  3. PPP2R5D-related intellectual disability 
    ... are associated with intellectual disability, macrocephaly, hypotonia, and autism. Neurogenetics. 2016 Jan;17(1):43-9. doi: 10.1007/s10048-015- ...
    https://medlineplus.gov/.../ppp2r5d-related-intellectual-disability - Genetics
  4. PPP2R5D gene 
    ... are associated with intellectual disability, macrocephaly, hypotonia, and autism. Neurogenetics. 2016 Jan;17(1):43-9. doi: 10.1007/s10048-015- ...
    https://medlineplus.gov/genetics/gene/ppp2r5d - Genetics
  5. Chromosome 16 
    ... WB, Christian SL. Recurrent 16p11.2 microdeletions in autism. Hum Mol Genet. 2008 Feb 15;17(4):628-38. doi: 10.1093/hmg/ddm376. ...
    https://medlineplus.gov/genetics/chromosome/16 - Genetics
  6. 16p11.2 deletion syndrome 
    ... WB, Christian SL. Recurrent 16p11.2 microdeletions in autism. Hum Mol Genet. 2008 Feb 15;17(4):628-38. doi: 10.1093/hmg/ddm376. ...
    https://medlineplus.gov/genetics/condition/16p112-deletion-syndrome - Genetics
  7. ADNP syndrome 
    ... unknown. It is estimated to account for 0.17 percent of all cases of autism spectrum disorder, making it one of the most ...
    https://medlineplus.gov/genetics/condition/adnp-syndrome - Genetics
  8. Jacobsen syndrome 
    ... Akshoomoff N, Mattson SN, Grossfeld PD. Evidence for autism spectrum disorder in Jacobsen syndrome: identification of a candidate gene in distal 11q. Genet Med. 2015 Feb;17(2):143-8. doi: 10.1038/gim.2014. ...
    https://medlineplus.gov/genetics/condition/jacobsen-syndrome - Genetics
  9. SHANK3 gene 
    ... the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders. Nat Genet. 2007 Jan;39(1):25-7. doi: 10.1038/ng1933. Epub 2006 Dec 17. Citation on PubMed or Free article on PubMed ...
    https://medlineplus.gov/genetics/gene/shank3 - Genetics
  10. RAI1 gene 
    ... by delayed development, mild to moderate intellectual disability, autism ... the short (p) arm of chromosome 17 at position p11.2. In about two-thirds ...
    https://medlineplus.gov/genetics/gene/rai1 - Genetics
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