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. 1982 Oct;19(5):387–388. doi: 10.1136/jmg.19.5.387

The hypertelorism microtia clefting syndrome

PMCID: PMC1048929 PMID: 7143395

Abstract

A single case of the hypertelorism microtia clefting (HMC) syndrome, a rare autosomal recessive condition, is reported.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

Bixler D., Christian J. C., Gorlin R. J. Hypertelorism, microtia, and facial clefting. A newly described inherited syndrome. Am J Dis Child. 1969 Sep;118(3):495–500. doi: 10.1001/archpedi.1969.02100040497015. [DOI] [PubMed] [Google Scholar]
Schweckendiek W., Hillig U., Kruse E., Rodeck G., Wendt G. G. HMC syndrome in identical twins. Hum Genet. 1976 Aug 30;33(3):315–318. doi: 10.1007/BF00286858. [DOI] [PubMed] [Google Scholar]

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