Whole-exome sequencing, without prior linkage, identifies a mutation in LAMB3 as a cause of dominant hypoplastic amelogenesis imperfecta

Enamel Defects in Carriers of a Novel LAMA3 Mutation Underlying Epidermolysis Bullosa

(2013) W Yuen et al.   ACTA DERMATO-VENEREOLOGICA

Mutations in C4orf26, Encoding a Peptide with In Vitro Hydroxyapatite Crystal Nucleation and Growth Activity, Cause Amelogenesis Imperfecta

(2012) David A. Parry et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Amelogenesis Imperfecta: Genotype-Phenotype Studies in 71 Families

(2011) J. Timothy Wright et al.   CELLS TISSUES ORGANS

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

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

FAM83H Mutations in Families with Autosomal-Dominant Hypocalcified Amelogenesis Imperfecta

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

Type XVII Collagen is a Key Player in Tooth Enamel Formation

(2008) Takuya Asaka et al.   AMERICAN JOURNAL OF PATHOLOGY

The genetic basis of inherited anomalies of the teeth

(2008) Isabelle Bailleul-Forestier et al.   European Journal of Medical Genetics

The multiple lives of NMD factors: balancing roles in gene and genome regulation

(2008) Olaf Isken et al.   NATURE REVIEWS GENETICS