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  • Sorting nexin 3 (SNX3) is disrupted in a patient with a translocation t(6;13)(q21;q12) and microcephaly, microphthalmia, ectrodactyly, prognathism (MMEP) phenotype

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Original article
Sorting nexin 3 (SNX3) is disrupted in a patient with a translocation t(6;13)(q21;q12) and microcephaly, microphthalmia, ectrodactyly, prognathism (MMEP) phenotype

Authors

  1. Correspondence to:
 Dr C Schwartz, J C Self Research Institute of Human Genetics, Greenwood Genetic Center, One Gregor Mendel Circle, Greenwood, SC 29646, USA;
 schwartz{at}ggc.org
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Citation

Vervoort VS, Viljoen D, Smart R, et al
Sorting nexin 3 (SNX3) is disrupted in a patient with a translocation t(6;13)(q21;q12) and microcephaly, microphthalmia, ectrodactyly, prognathism (MMEP) phenotype
Journal of Medical Genetics 2002;39:893-899.

Publication history

  • Accepted August 15, 2002
  • Revised August 15, 2002
  • First published December 1, 2002.
Online issue publication 
April 27, 2016

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Copyright 2002 Journal of Medical Genetics