The genetic basis of inherited anomalies of the teeth. Part 2: Syndromes with significant dental involvement

Author:

Bailleul-Forestier Isabelle,Berdal Ariane,Vinckier Frans,de Ravel Thomy,Fryns Jean Pierre,Verloes Alain

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics,General Medicine

Reference164 articles.

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3. Incontinentia pigmenti (IP2): familiar case report with affected men. Literature review;Arenas-Sordo;Med. Oral Patol. Oral Cir. Bucal.,2005

4. Immunolocalization of vitamin D receptor and calbindin-D28k in human tooth germ;Bailleul-Forestier;Pediatr. Res.,1996

5. The oro-dental phenotype in Prader–Willi syndrome: a survey of 15 patients;Bailleul-Forestier;Int. J. Paediatr. Dent.,2008

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