A novel mutation in the AMELX gene and multiple crown resorptions

Hypomaturation Amelogenesis Imperfecta due to WDR72 Mutations: A Novel Mutation and Ultrastructural Analyses of Deciduous Teeth

(2011) W. El-Sayed et al.   CELLS TISSUES ORGANS

Craniofacial characteristics and genotypes of amelogenesis imperfecta patients

(2010) A. Pavlic et al.   EUROPEAN JOURNAL OF ORTHODONTICS

Novel WDR72 Mutation and Cytoplasmic Localization

(2010) S.-K. Lee et al.   JOURNAL OF DENTAL RESEARCH

Altered Enamelin Phosphorylation Site Causes Amelogenesis Imperfecta

(2010) H.-C. Chan et al.   JOURNAL OF DENTAL RESEARCH

FAM83H Mutations Cause ADHCAI and Alter Intracellular Protein Localization

(2010) S.-K. Lee et al.   JOURNAL OF DENTAL RESEARCH

Human cementoblasts express enamel-associated molecules in vitro and in vivo

(2010) J. Nuñez et al.   JOURNAL OF PERIODONTAL RESEARCH

Mutations in the Beta Propeller WDR72 Cause Autosomal-Recessive Hypomaturation Amelogenesis Imperfecta

(2009) Walid El-Sayed et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Ultrastructural Analyses of Deciduous Teeth Affected by Hypocalcified Amelogenesis Imperfecta from a Family with a Novel Y458X FAM83H Nonsense Mutation

(2009) W. El-Sayed et al.   CELLS TISSUES ORGANS

NovelFAM83Hmutations in Turkish families with autosomal dominant hypocalcified amelogenesis imperfecta

(2009)   CLINICAL GENETICS

Identification of a novelFAM83Hmutation and microhardness of an affected molar in autosomal dominant hypocalcified amelogenesis imperfecta

(2009) H.-K. Hyun et al.   INTERNATIONAL ENDODONTIC JOURNAL

Premature Stop Codon in MMP20 Causing Amelogenesis Imperfecta

(2009) P. Papagerakis et al.   JOURNAL OF DENTAL RESEARCH

MMP20 Hemopexin Domain Mutation in Amelogenesis Imperfecta

(2009) S.-K. Lee et al.   JOURNAL OF DENTAL RESEARCH

The Amelogenin C-Terminus Is Required for Enamel Development

(2009) M.K. Pugach et al.   JOURNAL OF DENTAL RESEARCH

Candidate Gene Strategy Reveals ENAM Mutations

(2009) H.-Y. Kang et al.   JOURNAL OF DENTAL RESEARCH

Phenotypic Variation in FAM83H-associated Amelogenesis Imperfecta

(2009) J.T. Wright et al.   JOURNAL OF DENTAL RESEARCH

FAM83H Mutations in Families with Autosomal-Dominant Hypocalcified Amelogenesis Imperfecta

(2008) Jung-Wook Kim et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Mutational spectrum ofFAM83H: the C-terminal portion is required for tooth enamel calcification

(2008) Sook-Kyung Lee et al.   HUMAN MUTATION