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There are 30135 results for: content related to: The syndrome of ankyloblepharon, ectodermal defects and cleft lip and palate: an autosomal dominant condition

  1. 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

  2. Genetics and Genodermatoses

    Rook's Textbook of Dermatology, Seventh Edition

    J. I. Harper, R. C. Trembath, Pages: 383–468, 2008

    Published Online : 4 FEB 2008, DOI: 10.1002/9780470750520.ch12

  3. Ectodermal dysplasias

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

    Volume 131C, Issue 1, 15 November 2004, Pages: 45–51, Peter H. Itin and Susanna K. Fistarol

    Version of Record online : 5 OCT 2004, DOI: 10.1002/ajmg.c.30033

  4. Ectodermal Dysplasias

    Standard Article

    Rook's Textbook of Dermatology

    Peter Itin

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

  5. You have free access to this content
    Ectodermal dysplasias: An overview and update of clinical and molecular-functional mechanisms

    American Journal of Medical Genetics Part A

    Volume 149A, Issue 9, September 2009, Pages: 2003–2013, Manuela Priolo

    Version of Record online : 5 JUN 2009, DOI: 10.1002/ajmg.a.32804

  6. A Genetic Study of Hypohidrotic Ectodermal Dysplasia

    Pediatrics International

    Volume 24, Issue 3, September 1980, Pages: 372–379, Shozo Ohdo, Takuya Ikeda and Kunio Hayakawa

    Version of Record online : 9 OCT 2007, DOI: 10.1111/j.1442-200X.1980.tb00536.x

  7. Hypohidrotic Ectodermal Dysplasia: Argument Against an Autosomal Recessive Form Clinically Indistinguishable from X-Linked Hypohidrotic Ectodermal Dysplasia (Christ-Siemens-Touraine Syndrome)

    Pediatric Dermatology

    Volume 6, Issue 2, June 1989, Pages: 76–81, Virginia P. Sybert

    Version of Record online : 20 MAR 2008, DOI: 10.1111/j.1525-1470.1989.tb01002.x

  8. Christ-Siemens-Touraine syndrom—a clinical and genetic analysis of a large Brazilian kindred: III. Carrier detection

    American Journal of Medical Genetics

    Volume 4, Issue 2, 1979, Pages: 129–134, M. Pinheiro and N. Freire-Maia

    Version of Record online : 2 JUN 2005, DOI: 10.1002/ajmg.1320040204

  9. Unusual Cutaneous Manifestations of Anhidrotic Ectodermal Dysplasia

    The Journal of Dermatology

    Volume 17, Issue 6, June 1990, Pages: 380–384, Kirtikant C. Shah and Dipak D. Umrigar

    Version of Record online : 9 APR 2015, DOI: 10.1111/j.1346-8138.1990.tb01660.x

  10. Hereditary and Congenital Nail Disorders

    Baran & Dawber's Diseases of the Nails and their Management, Fourth Edition

    Smail Hadj-Rabia, Lennart Juhlin, Robert Baran, Pages: 485–547, 2012

    Published Online : 23 MAY 2012, DOI: 10.1002/9781118286715.ch11

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    2008 International Conference on Ectodermal Dysplasias Classification: Conference report

    American Journal of Medical Genetics Part A

    Volume 149A, Issue 9, September 2009, Pages: 1958–1969, Carlos F. Salinas, Ronald J. Jorgenson, J. Timothy Wright, John J. DiGiovanna and Mary D. Fete

    Version of Record online : 13 AUG 2009, DOI: 10.1002/ajmg.a.32882

  12. You have free access to this content
    Ectodermal dysplasias: Clinical and molecular review

    American Journal of Medical Genetics Part A

    Volume 149A, Issue 9, September 2009, Pages: 1980–2002, Átila F. Visinoni, Toni Lisboa-Costa, Nina A.B. Pagnan and Eleidi A. Chautard-Freire-Maia

    Version of Record online : 13 AUG 2009, DOI: 10.1002/ajmg.a.32864

  13. Hereditary and Congenital Nail Disorders

    Baran and Dawber's Diseases of the Nails and their Management, Third Edition

    L. Juhlin, R. Baran, Pages: 370–424, 2008

    Published Online : 16 APR 2008, DOI: 10.1002/9780470694947.ch9

  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. Etiology and pathogenesis of ectodermal dysplasias

    American Journal of Medical Genetics Part A

    Volume 164, Issue 10, October 2014, Pages: 2472–2477, Peter H. Itin

    Version of Record online : 8 APR 2014, DOI: 10.1002/ajmg.a.36550

  16. Hereditary Ectodermal Dysplasia of Anhidrotic Type with Increased Protein-Bound Serum Thyroxine

    Acta Paediatrica

    Volume 56, Issue 6, November 1967, Pages: 687–692, ERIK HIPPE

    Version of Record online : 21 JAN 2008, DOI: 10.1111/j.1651-2227.1967.tb15997.x

  17. Schöpf–Schulz–Passarge syndrome resulting from a homozygous nonsense mutation, p.Cys107X, in WNT10A

    Australasian Journal of Dermatology

    Volume 52, Issue 3, August 2011, Pages: 224–226, Gabriela Petrof, Kenneth Fong, Joey E Lai-Cheong, Sarah E Cockayne and John A McGrath

    Version of Record online : 29 JUN 2011, DOI: 10.1111/j.1440-0960.2011.00788.x

  18. Autosomal dominant anhidrotic ectodermal dysplasias at the EDARADD locus

    Human Mutation

    Volume 28, Issue 7, July 2007, Pages: 703–709, E. Bal, L. Baala, C. Cluzeau, F. El Kerch, K. Ouldim, S. Hadj-Rabia, C. Bodemer, A. Munnich, G. Courtois, A. Sefiani and A. Smahi

    Version of Record online : 12 MAR 2007, DOI: 10.1002/humu.20500

  19. ANHIDROTIC ECTODERMAL DYSPLASIA

    International Journal of Dermatology

    Volume 17, Issue 2, March 1978, Pages: 139–141, B. S. N. REDDY, SUSIL CHANDRA, P. K. JHA and GURMOHAN SINGH

    Version of Record online : 5 MAR 2008, DOI: 10.1111/j.1365-4362.1978.tb06124.x

  20. HEREDITARY ECTODERMAL DYSPLASIA

    Acta Paediatrica

    Volume 59, Issue 1, January 1970, Pages: 94–99, GÖSTA SAMUELSON

    Version of Record online : 21 JAN 2008, DOI: 10.1111/j.1651-2227.1970.tb15522.x