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May 27, 2008Orphanet Journal of Rare DiseasesOpen Access

Deletion 22q13.3 syndrome

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Authors

MPMary C. PhelanSt. Luke's General Hospital

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Cite This Study

Mary C. Phelan (2008) studied this question.

synapsesocial.com/papers/6a7c288aa7aadf9f7c3bd9bbhttps://doi.org/10.1186/1750-1172-3-14
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Also Consider

Synapse has enriched 3 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Further delineation of the 22q13 deletion syndrome2005 · 49 citations
  2. 2A familial pericentric inversion of chromosome 22 with a recombinant subject illustrating a 'pure' partial monosomy syndrome.1985 · 85 citations
  3. 3Subtelomere FISH analysis of 11 688 cases: an evaluation of the frequency and pattern of subtelomere rearrangements in individuals with developmental disabilities2005 · 413 citations