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May 1, 1982American Journal of Medical Genetics

Brief cytogenetic case report: A 4.5‐year‐old girl with deletion 4q syndrome — de novo, 46,XX, del(4) (pter→q31:)

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Authors

RYRobert S. YoungZhejiang University-University of Edinburgh InstituteCPCatherine G. PalmerUniversity Medical CenterHBHarvey A. BenderIcahn School of Medicine at Mount Sinai

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Young et al. (1982) studied this question.

synapsesocial.com/papers/6a9ffce66fb3bd2270351138https://doi.org/10.1002/ajmg.1320120114
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Also Consider

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

  1. 1The del(4) (q31) syndrome‐A recognizable disorder with atypical Robin malformation Sequence1981 · 21 citations
  2. 2Preferential location of X-ray induced chromosome breakage in the R-bands of human chromosomes2009 · 136 citations
  3. 3A patient with congenital anomalies and a deletion of the long arm of the long arm of chromosome 4 [46,XY,del(4)(q31)].1975 · 22 citations