Search Results

There are 11853 results for: content related to: Mutations in the EDA gene are responsible for X-linked hypohidrotic ectodermal dysplasia and hypodontia in Chinese kindreds

  1. A novel missense mutation in the ectodysplasin-A (EDA) gene underlies X-linked recessive nonsyndromic hypodontia

    International Journal of Dermatology

    Volume 49, Issue 12, December 2010, Pages: 1399–1402, Muhammad Ayub, Fazal Ur-Rehman, Masoom Yasinzai and Wasim Ahmad

    Version of Record online : 23 NOV 2010, DOI: 10.1111/j.1365-4632.2010.04596.x

  2. Novel EDA mutation in X-linked hypohidrotic ectodermal dysplasia and genotype–phenotype correlation

    Oral Diseases

    Volume 21, Issue 8, November 2015, Pages: 994–1000, B Zeng, H Lu, X Xiao, L Zhou, J Lu, L Zhu, D Yu and W Zhao

    Version of Record online : 24 OCT 2015, DOI: 10.1111/odi.12376

  3. 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

  4. Isolated oligodontia associated with mutations in EDARADD, AXIN2, MSX1, and PAX9 genes

    American Journal of Medical Genetics Part A

    Volume 155, Issue 7, July 2011, Pages: 1616–1622, Birgitta Bergendal, Joakim Klar, Christina Stecksén-Blicks, Johanna Norderyd and Niklas Dahl

    Version of Record online : 27 MAY 2011, DOI: 10.1002/ajmg.a.34045

  5. You have free access to this content
    From ectodermal dysplasia to selective tooth agenesis

    American Journal of Medical Genetics Part A

    Volume 149A, Issue 9, September 2009, Pages: 2037–2041, Gabriele I. Mues, Rachel Griggs, Andrew J. Hartung, Greg Whelan, Lyle G. Best, Anand K. Srivastava and Rena D'Souza

    Version of Record online : 5 JUN 2009, DOI: 10.1002/ajmg.a.32801

  6. Mutations in WNT10A are frequently involved in oligodontia associated with minor signs of ectodermal dysplasia

    American Journal of Medical Genetics Part A

    Volume 161, Issue 4, April 2013, Pages: 671–678, Julie Plaisancié, Isabelle Bailleul-Forestier, Véronique Gaston, Fréderic Vaysse, Didier Lacombe, Muriel Holder-Espinasse, Marc Abramowicz, Christine Coubes, Ghislaine Plessis, Laurence Faivre, Bénédicte Demeer, Catherine Vincent-Delorme, Hélène Dollfus, Sabine Sigaudy, Encarna Guillén-Navarro, Alain Verloes, Philippe Jonveaux, Dominique Martin-Coignard, Estelle Colin, Eric Bieth, Patrick Calvas and Nicolas Chassaing

    Version of Record online : 7 FEB 2013, DOI: 10.1002/ajmg.a.35747

  7. Dental agenesis: genetic and clinical perspectives

    Journal of Oral Pathology & Medicine

    Volume 38, Issue 1, January 2009, Pages: 1–17, P. J. De Coster, L. A. Marks, L. C. Martens and A. Huysseune

    Version of Record online : 3 SEP 2008, DOI: 10.1111/j.1600-0714.2008.00699.x

  8. Ectodermal Dysplasias

    Standard Article

    Rook's Textbook of Dermatology, Ninth Edition

    Peter Itin

    Published Online : 9 OCT 2016, DOI: 10.1002/9781118441213.rtd0068

  9. Ectodermal Dysplasias

    Harper's Textbook of Pediatric Dermatology, Volume 1, 2, Third Edition

    Yuka Asai, Alan D. Irvine, Pages: 127.1–127.104, 2011

    Published Online : 24 MAY 2011, DOI: 10.1002/9781444345384.ch127

  10. Mutations in EDARADD account for a small proportion of hypohidrotic ectodermal dysplasia cases

    British Journal of Dermatology

    Volume 162, Issue 5, May 2010, Pages: 1044–1048, N. Chassaing, C. Cluzeau, E. Bal, P. Guigue, M-C. Vincent, G. Viot, D. Ginisty, A. Munnich, A. Smahi and P. Calvas

    Version of Record online : 5 MAR 2010, DOI: 10.1111/j.1365-2133.2010.09670.x

  11. Orodental manifestations in ectodermal dysplasia—A review

    American Journal of Medical Genetics Part A

    Volume 164, Issue 10, October 2014, Pages: 2465–2471, Birgitta Bergendal

    Version of Record online : 9 APR 2014, DOI: 10.1002/ajmg.a.36571

  12. You have full text access to this OnlineOpen article
    Taurodontism, variations in tooth number, and misshapened crowns in Wnt10a null mice and human kindreds

    Molecular Genetics & Genomic Medicine

    Volume 3, Issue 1, January 2015, Pages: 40–58, Jie Yang, Shih-Kai Wang, Murim Choi, Bryan M. Reid, Yuanyuan Hu, Yuan-Ling Lee, Curtis R. Herzog, Hera Kim-Berman, Moses Lee, Paul J. Benke, K. C. Kent Lloyd, James P. Simmer and Jan C.-C. Hu

    Version of Record online : 15 SEP 2014, DOI: 10.1002/mgg3.111

  13. Unusual presentation of a severe autosomal recessive anhydrotic ectodermal dysplasia with a novel mutation in the EDAR gene

    American Journal of Medical Genetics Part A

    Volume 146A, Issue 20, 15 October 2008, Pages: 2657–2662, Hala Mégarbané, Céline Cluzeau, Christine Bodemer, Sylvie Fraïtag, Myrna Chababi-Atallah, André Mégarbané and Asma Smahi

    Version of Record online : 24 SEP 2008, DOI: 10.1002/ajmg.a.32509

  14. A founder ectodysplasin A receptor (EDAR) mutation results in a high frequency of the autosomal recessive form of hypohidrotic ectodermal dysplasia in India

    British Journal of Dermatology

    Volume 166, Issue 4, April 2012, Pages: 819–829, M.D. Bashyam, A.K. Chaudhary, E.C. Reddy, V. Reddy, V. Acharya, H.A. Nagarajaram, A.R.R. Devi, L. Bashyam, A.B. Dalal, N. Gupta, M. Kabra, M. Agarwal, S.R. Phadke, R. Tainwala, R. Kumar and S.V. Hariharan

    Version of Record online : 5 MAR 2012, DOI: 10.1111/j.1365-2133.2011.10707.x

  15. A novel Gln358Glu mutation in ectodysplasin A associated with X-linked dominant incisor hypodontia

    American Journal of Medical Genetics Part A

    Volume 143A, Issue 4, 15 February 2007, Pages: 390–394, Patrick Tarpey, Trevor J. Pemberton, David W. Stockton, Parimal Das, Vasiliki Ninis, Sarah Edkins, P. Andrew Futreal, Richard Wooster, Sushanth Kamath, Rabindra Nayak, Michael R. Stratton and Pragna I. Patel

    Version of Record online : 26 JAN 2007, DOI: 10.1002/ajmg.a.31567

  16. The pattern and prevalence of hypodontia in Koreans

    Oral Diseases

    Volume 14, Issue 7, October 2008, Pages: 620–625, CJ Chung, J-H Han and K-H Kim

    Version of Record online : 1 FEB 2008, DOI: 10.1111/j.1601-0825.2007.01434.x

  17. Dental Anomalies: Genetics

    Standard Article


    Pekka Nieminen

    Published Online : 15 MAR 2013, DOI: 10.1002/9780470015902.a0006088.pub2

  18. Two novel mutations in the gene EDAR causing autosomal recessive hypohidrotic ectodermal dysplasia

    Orthodontics & Craniofacial Research

    Volume 14, Issue 3, August 2011, Pages: 156–159, SK Naqvi, N Wasif, H Javaid and W Ahmad

    Version of Record online : 14 JUL 2011, DOI: 10.1111/j.1601-6343.2011.01521.x

  19. Developmental disorders of the dentition: An update

    American Journal of Medical Genetics Part C: Seminars in Medical Genetics

    Volume 163, Issue 4, November 2013, Pages: 318–332, Ophir D. Klein, Snehlata Oberoi, Ann Huysseune, Maria Hovorakova, Miroslav Peterka and Renata Peterkova

    Version of Record online : 4 OCT 2013, DOI: 10.1002/ajmg.c.31382

  20. X-linked and autosomal recessive Hypohidrotic Ectodermal Dysplasia: genotypic-dental phenotypic findings

    Clinical Genetics

    Volume 78, Issue 3, September 2010, Pages: 257–266, F Clauss, N Chassaing, A Smahi, MC Vincent, P Calvas, M Molla, H Lesot, Y Alembik, S Hadj-Rabia, C Bodemer, MC Manière and M Schmittbuhl

    Version of Record online : 24 FEB 2010, DOI: 10.1111/j.1399-0004.2010.01376.x