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September 18, 2001Proceedings of the National Academy of Sciences

Genetic factors are major determinants of phenotypic variability in a mouse model of the DiGeorge/ del22q11 syndromes

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ITIlaria TaddeiHôpital Necker-Enfants MaladesMMMasae MorishimaTokyo Women's Medical UniversityTHTuong HuynhBaylor College of Medicine

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Taddei et al. (2001) studied this question.

synapsesocial.com/papers/6a77ea46df493903fd1f5129https://doi.org/10.1073/pnas.201127298
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Also Consider

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

  1. 1Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis2000 · 531 citations
  2. 2A common molecular basis for rearrangement disorders on chromosome 22q111999 · 457 citations
  3. 3Submicroscopic deletions at 22q11.2: Variability of the clinical picture and delineation of a commonly deleted region1995 · 120 citations
  4. 4Molecular Definition of 22q11 Deletions in 151 Velo-Cardio-Facial Syndrome Patients1997 · 363 citations