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March 13, 1995American Journal of Medical Genetics

Upper limb malformations in DiGeorge syndrome

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Authors

VCValérie Cormier‐DaireHôpital Necker-Enfants MaladesLILaurence IserinAdult Congenital Heart DiseaseDTDidier Theophile

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Cite This Study

Cormier‐Daire et al. (1995) studied this question.

synapsesocial.com/papers/6aab9b09bf7b76dfa6834ce2https://doi.org/10.1002/ajmg.1320560111
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Also Consider

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

  1. 1Isolation of a putative transcriptional regulator from the region of 22q11 deleted in DiGeorge syndrome, Shprintzen syndrome and familial congenital heart disease1993 · 141 citations
  2. 2DiGeorge syndrome: part of CATCH 22.1993 · 511 citations
  3. 3Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis.1993 · 489 citations
  4. 4The DiGeorge anomaly as a developmental field defect1986 · 217 citations