| Literature DB >> 17001670 |
A Richieri-Costa1, Lucilene Arilho Ribeiro.
Abstract
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.Entities:
Mesh:
Year: 2006 PMID: 17001670 DOI: 10.1002/ajmg.a.31379
Source DB: PubMed Journal: Am J Med Genet A ISSN: 1552-4825 Impact factor: 2.802