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Variable expression in Amelogenesis imperfecta with taurodontismALRED, M. J; CRAWFORD, P. J. M.Journal of oral pathology. 1988, Vol 17, Num 5, pp 327-333, issn 0300-9777Article

Amelogenesis imperfecta, dentinogenesis imperfecta and dentin dysplasia revisited: problems in classificationWITKOP, C. J. JR.Journal of oral pathology. 1988, Vol 17, Num 9-10, pp 547-553, issn 0300-9777Article

X-LINKED RECESSIVE HYPOMATURATION AMELOGENESIS IMPERFECTA: REPORT OF CASEHAUG RH; FERGUSON FS.1981; J. AM. DENT. ASSOC.; ISSN 0002-8177; USA; DA. 1981; VOL. 102; NO 6; PP. 865-867; BIBL. 7 REF.Article

Amelogenesis imperfecta with taurodontism and the tricho-dento-osseous syndrome : separate conditions or a spectrum of disease ?CRAWFORD, P. J. M; ALDRED, M. J.Clinical genetics. 1990, Vol 38, Num 1, pp 44-50, issn 0009-9163, 7 p.Article

Amelogenesis imperfecta: a genetic studyBACKMAN, B; HOLMGREN, G.Human heredity. 1988, Vol 38, Num 4, pp 189-206, issn 0001-5652Article

Autosomal recessive rough hypoplastic amelogenesis imperfecta: a case report with clinical, light microscopic, radiographic, and electron microscopic observationsOOYA, K; NALBANDIAN, J; NOIKURA, T et al.Oral surgery, oral medicine, oral pathology. 1988, Vol 65, Num 4, pp 449-458, issn 0030-4220Article

AN ESTHETIC TRANSITIONAL TREATMENT FOR AMELOGENESIS IMPERFECTA: REPORT OF TWO CASES.LIGHT EI; RAKOW B; FRAZE RL et al.1975; J. AMER. DENT. ASS.; U.S.A.; DA. 1975; VOL. 90; NO 1; PP. 166-170; BIBL. 15 REF.Article

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

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

AMELOGENESIS IMPERFECTA AMONG ISRAELI JEWS AND THE DESCRIPTION OF A NEW TYPE OF LOCAL HYPOPLASTIC AUTOSOMAL RECESSIVE AMELOGENESIS IMPERFECTACHOSACK A; EIDELMAN E; WISOTSKI I et al.1979; ORAL SURG. ORAL MED. ORAL PATHOL.; USA; DA. 1979; VOL. 47; NO 2; PP. 148-156; BIBL. 13 REF.Article

AMELOGENESIS IMPERFECTA WITH TAURODONTISMCONGLETON J; BURKES EJ JR.1979; ORAL SURG. ORAL MED. ORAL PATHOL.; USA; DA. 1979; VOL. 48; NO 6; PP. 540-544; BIBL. 16 REF.Article

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

Open bite deformity in amelogenesis imperfecta. Part 2 : Le Fort I osteotomies and treatment resultsHOPPENREIJS, T. J. M; VOORSMIT, R. A. C. A; FREIHOFER, H. P. M et al.Journal of cranio-maxillo-facial surgery. 1998, Vol 26, Num 5, pp 286-293, issn 1010-5182Article

Molecular basis and consequences of a deletion in the amelogenin gene, analyzed by capture PCRLAGERSTRÖM-FERMER, M; PETTERSSON, U; LANDEGREN, U et al.Genomics (San Diego, Calif.). 1993, Vol 17, Num 1, pp 89-92, issn 0888-7543Article

Enamel ultrastructure in pigmented hypomaturation amelogenesis imperfectaTIMOTHY WRIGHT, J; LORD, V; ROBINSON, C et al.Journal of oral pathology & medicine. 1992, Vol 21, Num 9, pp 390-394, issn 0904-2512Article

A progressive cone-rod dystrophy and amelogenesis imperfecta: a new syndromeJALILI, I. K; SMITH, M. J. D.Journal of medical genetics. 1988, Vol 25, Num 11, pp 738-740, issn 0022-2593Article

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

Clinical and radiographic features of a family with autosomal dominant amelogenesis imperfecta with taurodontismALDRED, M. J; SAVARIRAYAN, R; LAMANDE, S. R et al.Oral diseases. 2002, Vol 8, Num 1, pp 62-68, issn 1354-523XArticle

Molecular analysis for genetic counselling in amelogenesis imperfectaALDRED, M. J; HALL, R. K; KILPATRICK, N et al.Oral diseases. 2002, Vol 8, Num 5, pp 249-253, issn 1354-523XArticle

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