A newly recognized syndrome of cutis aplasia, lipomatous footpads, microcephaly, hypotelorism, and, variably, single maxillary central incisor, and holoprosencephaly.

Source:http://linkedlifedata.com/resource/pubmed/id/15971262

Am. J. Med. Genet. A 2005 Aug 1 136A 4 354-6

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PMID
15971262