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Amelogenesis imperfecta: signs that should alert pediatric dentists = Amélogénèse imparfaite: signes d'alerte pour les pédodontistesTAKTAK, Najla; MANSOUR, Lamia; SIOUD, Sameh et al.MBCB. Médecine buccale chirurgie buccale. 2011, Vol 17, Num 1, pp 65-67, issn 1273-2761, 3 p.Article

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Exclusion of Candidate Genes in Seven Turkish Famities With Autosomal Recessive Amelogenesis mperfectaBECERIK, Sema; COGULU, Dilsah; EMINGIL, Gülnur et al.American journal of medical genetics. Part A. 2009, Vol 149, Num 7, pp 1392-1398, issn 1552-4825, 7 p.Article

The Use of Mouse Models to Investigate Shear Bond Strength in Amelogenesis ImperfectaPUGACH, M. K; OZER, F; LINDEMEYER, R. G et al.Journal of dental research. 2011, Vol 90, Num 11, pp 1352-1357, issn 0022-0345, 6 p.Article

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Whole-Exome Sequencing Identifies FAM20A Mutations as a Cause of Amelogenesis Imperfecta and Gingival Hyperplasia SyndromeO'SULLIVAN, James; BITU, Carolina C; COLETTA, Ricardo D et al.American journal of human genetics. 2011, Vol 88, Num 5, pp 616-620, issn 0002-9297, 5 p.Article

Enamelin (Enam) is essential for amelogenesis : ENU-induced mouse mutants as models for different clinical subtypes of human amelogenesis imperfecta (Al)MASUYA, Hiroshi; SHIMIZU, Kunihiko; KOBAYASHI, Kimio et al.Human molecular genetics (Print). 2005, Vol 14, Num 5, pp 575-583, issn 0964-6906, 9 p.Article

A spontaneous mutation: Amelogenesis imperfecta with cysts in ratsKATSUTA, Osamu; HOSHINO, Nobuhito; TAKEDA, Midori et al.Toxicologic pathology. 2003, Vol 31, Num 4, pp 411-416, issn 0192-6233, 6 p.Article

A new form of skeletal dysplasia with amelogenesis imperfecta and platyspondylyVERLOES, A; JAMBLIN, P; KOULISCHER, L et al.Clinical genetics. 1996, Vol 49, Num 1, pp 2-5, issn 0009-9163Article

Kohlschütter syndrome: syndrome of epilepsy-dementia-amelogenesis imperfectaPETERMÖLLER, M; KUNZE, J; GROSS-SELBECK, G et al.Neuropediatrics. 1993, Vol 24, Num 6, pp 337-338, issn 0174-304XArticle

Autosomal dominant amelogenesis imperfecta associated with ENAM frameshift mutation p.Asn36Ilefs56SIMMER, S. G; ESTRELLA, Nmrp; MILKOVICH, R. N et al.Clinical genetics. 2013, Vol 83, Num 2, pp 195-197, issn 0009-9163, 3 p.Article

Brachyolmia With Amelogenesis Imperfecta : Further Evidence of a Distinct EntityBERTOLA, D. R; ANTEQUERA, R; RODOVALHO, M. J et al.American journal of medical genetics. Part A. 2009, Vol 149, Num 3, pp 532-534, issn 1552-4825, 3 p.Article