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The hypertelorism microtia clefting syndrome.

Abstract
A single case of the hypertelorism microtia clefting (HMC) syndrome, a rare autosomal recessive condition, is reported.
AuthorsM Baraitser
JournalJournal of medical genetics (J Med Genet) Vol. 19 Issue 5 Pg. 387-8 (Oct 1982) ISSN: 0022-2593 [Print] England
PMID7143395 (Publication Type: Case Reports, Journal Article)
Topics
  • Cleft Lip (genetics)
  • Cleft Palate (genetics)
  • Craniofacial Dysostosis (genetics)
  • Ear, External (abnormalities)
  • Humans
  • Hypertelorism (genetics)
  • Infant, Newborn
  • Male
  • Syndrome

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