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The molecular etiologies and associated phenotypes of amelogenesis imperfectaWRIGHT, J. Timothy.American journal of medical genetics. Part A. 2006, Vol 140, Num 23, pp 2547-2555, issn 1552-4825, 9 p.Conference Paper

Novel ENAM mutation responsible for autosomal recessive amelogenesis imperfecta and localised enamel defectsHART, T. C; HART, P. S; GORRY, M. C et al.Journal of medical genetics. 2003, Vol 40, Num 12, pp 900-906, issn 0022-2593, 7 p.Article

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MMP-20 mutation in autosomal recessive pigmented hypomaturation amelogenesis imperfectaKIM, J.-W; SIMMER, J. P; HART, T. C et al.Journal of medical genetics. 2005, Vol 42, Num 3, pp 271-275, issn 0022-2593, 5 p.Article

Mutation of the signal peptide region of the bicistronic gene DSPP affects translocation to the endoplasmic reticulum and results in defective dentine biomineralizationRAJPAR, M. Helen; KOCH, Martin J; DAVIES, Robin M et al.Human molecular genetics (Print). 2002, Vol 11, Num 21, pp 2559-2565, issn 0964-6906Article

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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

FAM83H Mutations Cause ADHCAI and Alter Intracellular Protein LocalizationLEE, S.-K; LEE, K.-E; JEONG, T.-S et al.Journal of dental research. 2011, Vol 90, Num 3, pp 377-381, issn 0022-0345, 5 p.Article

Interdisciplinary treatment for a patient with open-bite malocclusion and amelogenesis imperfectaLUIZ RAMOS, Adilson; CORREA PASCOTTO, Renata; IWAKI FILHO, Liogi et al.American journal of orthodontics and dentofacial orthopedics. 2011, Vol 139, Num 4, issn 0889-5406, S145-S153, SUP1Article

Mutations in the Beta Propeller WDR72 Cause Autosomal-Recessive Hypomaturation Amelogenesis ImperfectaEL-SAYED, Walid; PARRY, David A; MIGHELL, Alan J et al.American journal of human genetics. 2009, Vol 85, Num 5, pp 699-705, issn 0002-9297, 7 p.Article

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It's only teeth: are there limits to genetic testing?ALDRED, M. J; CRAWFORD, P. J. M; SAVARIRAYAN, R et al.Clinical genetics. 2003, Vol 63, Num 5, pp 333-339, issn 0009-9163, 7 p.Article

A nonsense mutation in the enamelin gene causes local hypoplastic autosomal dominant amelogenesis imperfecta (AlH2)MARDH, Carina K; BÄCKMAN, Birgitta; HOLMGREN, Gösta et al.Human molecular genetics (Print). 2002, Vol 11, Num 9, pp 1069-1074, issn 0964-6906Article

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Clinical features of a family with X-linked amelogenesis imperfecta mapping to a new locus (AIH3) on the long arm of the X chromosomeCRAWORD, P. J. M; ALDRED, M. J.Oral surgery, oral medicine, oral pathology. 1993, Vol 76, Num 2, pp 187-191, issn 0030-4220Article