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June 7, 2012American Journal of Medical Genetics Part AOpen Access

Molecular characterization of 1q44 microdeletion in 11 patients reveals three candidate genes for intellectual disability and seizures

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Authors

GTGaëlle ThierryCBClaire BénéteauOPOlivier Pichon

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Thierry et al. (2012) studied this question.

synapsesocial.com/papers/6a92528b7c014fba2a435abahttps://doi.org/10.1002/ajmg.a.35423
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Also Consider

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

  1. 1Submicroscopic subtelomeric 1qter deletions: a recognisable phenotype?2001 · 65 citations
  2. 2A haplotype map of the human genome2005 · 5,960 citations
  3. 3Clinical and molecular characteristics of 1qter microdeletion syndrome: delineating a critical region for corpus callosum agenesis/hypogenesis2008 · 98 citations