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Craniofacial anomalies, cataracts, congenital heart disease, sacral neural tube defects, and growth and developmental retardation in two sisters: a new autosomal recessive MCA/MR syndrome?
  1. Correspondence to:
 Professor A S Teebi, Section of Clinical Genetics and Dysmorphology, Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, 555 University Avenue, Toronto, ON M5G 1X8, Canada;
 ateebi{at}sickkids.on.ca
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Siegel-Bartlet J, Levin A, Teebi AS, et al
Craniofacial anomalies, cataracts, congenital heart disease, sacral neural tube defects, and growth and developmental retardation in two sisters: a new autosomal recessive MCA/MR syndrome?

Publication history

  • First published February 1, 2002.
Online issue publication 
February 01, 2002

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