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1. Single maxillary central incisor, holoprosencephaly, and holoprosencephaly-like phenotype.
Match Strength: 19.708
Three patients--one with alobar holoprosencephaly and two with a holoprosencephaly-like phenotype--are reported with no identifiable mutations. In each case, one parent had a single maxillary central incisor (SMCI). We briefly review the holoprosencephaly-like phenotype and present a table of 25 conditions with SMCI. Publication Types: Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov ... Read More »
» Published in Am J Med Genet A. 2006 Dec 1;140(23):2594-7.
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