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There are 169729 results for: content related to: Novel FAM20A mutations in hypoplastic amelogenesis imperfecta

  1. Target gene analyses of 39 amelogenesis imperfecta kindreds

    European Journal of Oral Sciences

    Volume 119, Issue s1, December 2011, Pages: 311–323, Hui-Chen Chan, Ninna M. R. P. Estrella, Rachel N. Milkovich, Jung-Wook Kim, James P. Simmer and Jan C-C. Hu

    Version of Record online : 13 JAN 2012, DOI: 10.1111/j.1600-0722.2011.00857.x

  2. The Protein Composition of Normal and Developmentally Defective Enamel

    Ciba Foundation Symposium 205 - Dental Enamel

    J. Tim Wright, Kathie Hall, Mitsuo Yamauchi, Pages: 85–106, 2007

    Published Online : 28 SEP 2007, DOI: 10.1002/9780470515303.ch7

  3. Molecular Biology of Hereditary Enamel Defects

    Ciba Foundation Symposium 205 - Dental Enamel

    Michael J. Aldred, Peter J. M. Crawford, Pages: 200–211, 2007

    Published Online : 28 SEP 2007, DOI: 10.1002/9780470515303.ch14

  4. Inherited Enamel Defects

    Ciba Foundation Symposium 205 - Dental Enamel

    Derek J. Chadwick, Gail Cardew, Pages: 175–186, 2007

    Published Online : 28 SEP 2007, DOI: 10.1002/9780470515303.ch12

  5. The molecular etiologies and associated phenotypes of amelogenesis imperfecta

    American Journal of Medical Genetics Part A

    Volume 140A, Issue 23, 1 December 2006, Pages: 2547–2555, J. Timothy Wright

    Version of Record online : 12 JUL 2006, DOI: 10.1002/ajmg.a.31358

  6. A novel mutation in the AMELX gene and multiple crown resorptions

    European Journal of Oral Sciences

    Volume 119, Issue s1, December 2011, Pages: 324–328, Kyung-Eun Lee, Sook-Kyung Lee, Seung-Eun Jung, Su Jeong Song, Sang Hyun Cho, Zang Hee Lee and Jung-Wook Kim

    Version of Record online : 13 JAN 2012, DOI: 10.1111/j.1600-0722.2011.00858.x

  7. Diseases of the tooth: the genetic and molecular basis of inherited anomalies affecting the dentition

    Wiley Interdisciplinary Reviews: Developmental Biology

    Volume 2, Issue 2, March/April 2013, Pages: 183–212, Martyn T. Cobourne and Paul T. Sharpe

    Version of Record online : 25 MAY 2012, DOI: 10.1002/wdev.66

  8. Characterisation of molecular defects in X-linked amelogenesis imperfecta (AIH1)

    Human Mutation

    Volume 5, Issue 3, 1995, Pages: 251–259, Nicholas J. Lench and Gerald B. Winter

    Version of Record online : 1 JUN 2005, DOI: 10.1002/humu.1380050310

  9. Enamelin maps to human chromosome 4q21 within the autosomal dominant amelogenesis imperfecta locus

    European Journal of Oral Sciences

    Volume 108, Issue 5, October 2000, Pages: 353–358, J. Dong, T. T Gu, D. Simmons and M. MacDougall

    Version of Record online : 9 OCT 2008, DOI: 10.1034/j.1600-0722.2000.108005353.x

  10. Esthetic Treatment of a Diffuse Amelogenesis Imperfecta Using Pressed Lithium Disilicate and Feldspathic Ceramic Restorations: 5-Year Follow Up

    Journal of Esthetic and Restorative Dentistry

    Volume 26, Issue 6, November/December 2014, Pages: 363–373, Andrea Savi, Oliviero Turillazzi, Aldo Crescini and Maddalena Manfredi

    Version of Record online : 23 APR 2014, DOI: 10.1111/jerd.12104

  11. You have free access to this content
    Interventions for the restorative care of amelogenesis imperfecta in children and adolescents

    Intervention Review

    The Cochrane Library

    Mayssoon Dashash, C Albert Yeung, Issam Jamous and Anthony Blinkhorn

    Published Online : 6 JUN 2013, DOI: 10.1002/14651858.CD007157.pub2

  12. Amelogenesis imperfecta: a scanning electron microscopic and microradiographic study

    Journal of Oral Pathology & Medicine

    Volume 18, Issue 3, March 1989, Pages: 140–145, Birgitta Bäckman, Göran Anneroth and Per Hörstedt

    Version of Record online : 28 APR 2006, DOI: 10.1111/j.1600-0714.1989.tb00752.x

  13. Fine structure of the secretory and nonsecretory ameloblasts in the frog. I. Fine structure of the secretory ameloblasts

    American Journal of Anatomy

    Volume 148, Issue 2, February 1977, Pages: 161–193, A. E. Zaki and Dr. Edith K. MacRae

    Version of Record online : 3 FEB 2005, DOI: 10.1002/aja.1001480202

  14. Amelogenesis imperfecta – clinical manifestations in 51 families in a northern Swedish county

    European Journal of Oral Sciences

    Volume 96, Issue 6, December 1988, Pages: 505–516, BIRGITTA BÄCKMAN

    Version of Record online : 1 OCT 2007, DOI: 10.1111/j.1600-0722.1988.tb01590.x

  15. DLX3 mutation associated with autosomal dominant amelogenesis imperfecta with taurodontism

    American Journal of Medical Genetics Part A

    Volume 133A, Issue 2, 1 March 2005, Pages: 138–141, Juan Dong, David Amor, Michael J. Aldred, TingTing Gu, Michael Escamilla and Mary MacDougall

    Version of Record online : 21 JAN 2005, DOI: 10.1002/ajmg.a.30521

  16. Mutational analysis of candidate genes in 24 amelogenesis imperfecta families

    European Journal of Oral Sciences

    Volume 114, Issue s1, May 2006, Pages: 3–12, Jung-Wook Kim, James P. Simmer, Brent P.-L. Lin, Figen Seymen, John D. Bartlett and Jan C.-C. Hu

    Version of Record online : 2 MAY 2006, DOI: 10.1111/j.1600-0722.2006.00278.x

  17. Microradiographic study of amelogenesis imperfecta

    European Journal of Oral Sciences

    Volume 97, Issue 4, August 1989, Pages: 316–329, BIRGITTA BÄCKMAN and GÖRAN ANNEROTH

    Version of Record online : 1 OCT 2007, DOI: 10.1111/j.1600-0722.1989.tb01619.x

  18. You have full text access to this OnlineOpen article
    Novel ITGB6 mutation in autosomal recessive amelogenesis imperfecta

    Oral Diseases

    Volume 21, Issue 4, May 2015, Pages: 456–461, F Seymen, K-E Lee, M Koruyucu, K Gencay, M Bayram, EB Tuna, ZH Lee and J-W Kim

    Version of Record online : 19 JAN 2015, DOI: 10.1111/odi.12303

  19. You have full text access to this OnlineOpen article
    Is the 32-kDa fragment the functional enamelin unit in all species?

    European Journal of Oral Sciences

    Volume 119, Issue s1, December 2011, Pages: 345–350, Steven J. Brookes, Nicola J. Kingswell, Martin J. Barron, Michael J. Dixon and Jennifer Kirkham

    Version of Record online : 13 JAN 2012, DOI: 10.1111/j.1600-0722.2011.00869.x

  20. You have free access to this content
    Adaptor protein complex 2–mediated, clathrin-dependent endocytosis, and related gene activities, are a prominent feature during maturation stage amelogenesis

    Journal of Bone and Mineral Research

    Volume 28, Issue 3, March 2013, Pages: 672–687, Rodrigo S Lacruz, Steven J Brookes, Xin Wen, Jaime M Jimenez, Susanna Vikman, Ping Hu, Shane N White, S Petter Lyngstadaas, Curtis T Okamoto, Charles E Smith and Michael L Paine

    Version of Record online : 15 FEB 2013, DOI: 10.1002/jbmr.1779