Terminal 22q deletion syndrome: a newly recognized cause of speech and language disability in the autism spectrum.

No abstract is available for this paper.

• Publication year

  2004

• Venue

  Pediatrics

• Publication date

  2004-08-01

• Fields of study

  Medicine

• Identifiers
  DOI 10.1542/PEDS.114.2.451PMID 15286229
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• LETTERS TO THE EDITOR Detection of a familial cryptic translocation by fluorescent in situ hybridisation

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• Two novel human RAB genes with near identical sequence each map to a telomere-associated region: the subtelomeric region of 22q13.3 and the ancestral telomere band 2q13.

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