## 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 tabl
Holoprosencephaly-like phenotype: Clinical and genetic perspectives
✍ Scribed by A. Richieri-Costa; Lucilene Arilho Ribeiro
- Book ID
- 102701029
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 522 KB
- Volume
- 140A
- Category
- Article
- ISSN
- 1552-4825
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