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January 1, 2004Clinical Pediatrics

22q13 Deletion Syndrome: An Update and Review for the Primary Pediatrician

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Authors

JHJoaquim M. HavensJVJeannie VisootsakMPMary C. Phelan

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Cite This Study

Havens et al. (2004) studied this question.

synapsesocial.com/papers/6a89b6a96fc170cbc2fbbab7https://doi.org/10.1177/000992280404300106
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Also Consider

Synapse has enriched 4 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Case with autistic syndrome and chromosome 22q13.3 deletion detected by FISH2000 · 63 citations
  2. 2Multiple congenital anomaly/mental retardation (MCA/MR) syndrome with Goldenhar complex due to a terminal del(22q)1988 · 78 citations
  3. 3Evolution of Epilepsy and EEG Findings in Angelman Syndrome1997 · 147 citations
  4. 4A familial pericentric inversion of chromosome 22 with a recombinant subject illustrating a 'pure' partial monosomy syndrome.1985 · 84 citations