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Single maxillary central incisor, holoprosencephaly, and holoprosencephaly-like phenotype

✍ Scribed by A. Richieri-Costa; Lucilene Arilho Ribeiro

Book ID
101448316
Publisher
John Wiley and Sons
Year
2006
Tongue
English
Weight
205 KB
Volume
140A
Category
Article
ISSN
1552-4825

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✦ Synopsis

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. © 2006 Wiley‐Liss, Inc.

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