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November 1, 1983American Journal of Medical Genetics

A familial reciprocal translocation t(3;7) (p21.1;p13) associated with the Greig polysyndactyly‐craniofacial anomalies syndrome

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Authors

NTNiels TommerupUniversity of CopenhagenFNFrank NielsenKolding HospitalJohn M. OpitzJohn M. OpitzUniversity of Siena

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Tommerup et al. (1983) studied this question.

synapsesocial.com/papers/6a91afec51ec456f0643db2bhttps://doi.org/10.1002/ajmg.1320160304
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Also Consider

Synapse has enriched 2 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1The greig cephalopolysyndactyly syndrome in a canadian family1982 · 18 citations
  2. 2Molecular cloning and chromosomal mapping of a human locus related to the transforming gene of Moloney murine sarcoma virus.1982 · 65 citations