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Journal of Medical Genetics 1991;28:479-481; doi:10.1136/jmg.28.7.479
Copyright © 1991 by the BMJ Publishing Group Ltd.

Bilateral split hand and split foot malformation in a boy with a de novo interstitial deletion of 7q21.3

S H Roberts, H E Hughes, S J Davies, A L Meredith

Institute of Medical Genetics, University Hospital of Wales, Heath Park, Cardiff CF4 4XN.

A case of bilateral split hand and split foot malformation is reported in a boy with a complex rearrangement of chromosome 7 including a de novo interstitial deletion of 7q21.3.


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  • Duijf, P. H.G., van Bokhoven, H., Brunner, H. G. (2003). Pathogenesis of split-hand/split-foot malformation. Hum Mol Genet 12: R51-60 [Abstract] [Full Text]  
  • Vervoort, V S, Viljoen, D, Smart, R, Suthers, G, DuPont, B R, Abbott, A, Schwartz, C E (2002). Sorting nexin 3 (SNX3) is disrupted in a patient with a translocation t(6;13)(q21;q12) and microcephaly, microphthalmia, ectrodactyly, prognathism (MMEP) phenotype. J. Med. Genet. 39: 893-899 [Abstract] [Full Text]  
  • (1992). A comprehensive genetic linkage map of the human genome. NIH/CEPH Collaborative Mapping Group. Science 258: 67-86 [Abstract]  

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