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Limited phenotypic variation of hypocalcified amelogenesis imperfecta in a Danish five-generation family with a novel FAM83H nonsense mutation

✍ Scribed by DORTE HAUBEK; HANS GJØRUP; LILLIAN G. JENSEN; INGER JUNCKER; METTE NYEGAARD; ANDERS D. BØRGLUM; SVEN POULSEN; JENS M. HERTZ


Book ID
108829652
Publisher
John Wiley and Sons
Year
2011
Tongue
English
Weight
395 KB
Volume
21
Category
Article
ISSN
0960-7439

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