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March 29, 1996American Journal of Medical Genetics

Chromosome 22q11.2 deletion in a boy with Opitz (G/BBB) syndrome

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Authors

JFJulie S. FryburgKLKant Y. LinWGWendy L. Golden

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Cite This Study

Fryburg et al. (1996) studied this question.

synapsesocial.com/papers/6a96e14565cd0d1d26bb7bcbhttps://doi.org/10.1002/(sici)1096-8628(19960329)62:3<274::aid-ajmg13>3.0.co;2-h
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Also Consider

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

  1. 1Opitz GBBB syndrome: Chromosomal evidence of an X‐linked form1995 · 16 citations
  2. 2Distal deletion of chromosome 13 in a child with the “Opitz” GBBB syndrome1995 · 11 citations
  3. 3The telecanthus-hypospadias syndrome.1988 · 27 citations
  4. 4Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11.1993 · 270 citations