Amelogenesis imperfecta: a classification and catalogue for the 21st century von Aldred, MJ, Savarirayan, R, Crawford, PJM

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DLX3 mutation associated with autosomal dominant amelogenesis imperfecta with taurodontism von Dong, Juan, Amor, David, Aldred, Michael J., Gu, TingTing, Escamilla, Michael, MacDougall, Mary

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The patient with recurrent oral ulceration von Talacko, AA, Gordon, AK, Aldred, MJ

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Relationship of Phenotype and Genotype in X-Linked Amelogenesis Imperfecta von Wright, J. T., Hart, P. S., Aldred, M. J., Seow, K., Crawford, P. J. M., Hong, S. P., Gibson, C. W., Hart, T. C.

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Amelogenesis imperfecta phenotype–genotype correlations with two amelogenin gene mutations von Hart, P.S., Aldred, M.J., Crawford, P.J.M., Wright, N.J., Hart, T.C., Wright, J.T.

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Juvenile mandibular chronic osteomyelitis: a distinct clinical entity von Heggie, A

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It's only teeth - are there limits to genetic testing? von Aldred, MJ, Crawford, PJM, Savarirayan, R, Savulescu, J

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Identification of a locus on chromosome 2q11 at which recessive amelogenesis imperfecta and cone-rod dystrophy cosegregate von Downey, Louise M, Keen, T Jeffrey, Jalili, Ismail K, McHale, John, Aldred, Michael J, Robertson, Steven P, Mighell, Alan, Fayle, Steven, Wissinger, Bernd, Inglehearn, Chris F

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Oral focal mucinosis: report of two cases with ulceration von Talacko, Anna A., Lacy, Michael F., Besly, William J., Aldred, Michael J.

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Oral focal mucinosis: report of 15 cases and review of the literature von Aldred, Michael J., Talacko, Anna A., Ruljancich, Kevin, Story, Rowan D., Newland, Stuart, Chen, Stephen T., O’Grady, John F., Bergman, John D., Smith, Andrew, Dimitroulis, George, Redman, John, Sheldon, William R., Mansour, Alan K., Watkins, Don, Radden, Bryan G.

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Dental findings in a family with hyperparathyroidism-jaw tumor syndrome and a novel HRPT2 gene mutation von ALDRED, Michael J, TALACKO, Anna A, SAVARIRAYAN, Ravi, MURDOLO, Vince, MILLS, Alan E, RADDEN, Bryan G, ALIMOV, Andrei, VILLABLANCA, Andrea, LARSSON, Catharina

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'It's (not) only teeth' von Crawford, PJM, Aldred, MJ, Savarirayan, R, Savulescu, J

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Jaw lesions and hyperparathyroidism von Aldred, Michael J, Talacko, Anna A, Savarirayan, Ravi

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Identification of a nonsense mutation in the amelogenin gene (AMELX) in a family with X-linked amelogenesis imperfecta (AIH1) von Aldred, M J, Crawford, P J, Roberts, E, Thomas, N S

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Tricho-dento-osseous syndrome and amelogenesis imperfecta with taurodontism are genetically distinct conditions von Price, JA, Wright, JT, Walker, SJ, Crawford, PJM, Aldred, MJ, Hart, TC

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Odontogenic cyst with verrucous proliferation von Aldred, Michael J, Talacko, Anna A, Allan, Peter G, Shear, Mervyn

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Genetic disorders of the gingivae and periodontium von Aldred, Michael J., Bartold, P. Mark

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Clinical and radiographic features of a family with autosomal dominant amelogenesis imperfecta with taurodontism von Aldred, MJ, Savarirayan, R, Lamandé, SR, Crawford, PJM

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Clinical and radiographic dental findings in X linked hypohidrotic ectodermal dysplasia von Crawford, P J, Aldred, M J, Clarke, A

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Enamel defects and Lyonization in focal dermal hypoplasia von Balmer, Richard, Cameron, Angus C., Adès, Lesley, Aldred, Michael J.

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