American Journal of Medical Genetics Part A

Cover image for American Journal of Medical Genetics Part A

Special Issue: Thirteenth Annual Robert J. Gorlin Conference on Dysmorphology; Facial and Oral Structures: Molecular Perspectives

1 December 2006

Volume 140A, Issue 23

Pages 2511–2706

Issue edited by: M. Michael Cohen Jr.

  1. Introduction

    1. Top of page
    2. Introduction
    3. In Memoriam
    4. Research Articles
    5. Research Reviews
    6. Research Articles
    7. Clinical Reports
    8. Research Articles
    9. Clinical Reports
    10. Research Reviews
    11. New Syndrome
    12. Research Reviews
    1. You have free access to this content
      Robert J. Gorlin and the dysmorphology conferences (pages 2511–2512)

      M. Michael Cohen Jr

      Version of Record online: 25 SEP 2006 | DOI: 10.1002/ajmg.a.31357

  2. In Memoriam

    1. Top of page
    2. Introduction
    3. In Memoriam
    4. Research Articles
    5. Research Reviews
    6. Research Articles
    7. Clinical Reports
    8. Research Articles
    9. Clinical Reports
    10. Research Reviews
    11. New Syndrome
    12. Research Reviews
    1. In memoriam: Robert J. Gorlin, 1923–2006 (page 2513)

      Guilan Norouzi

      Version of Record online: 6 NOV 2006 | DOI: 10.1002/ajmg.a.31554

  3. Research Articles

    1. Top of page
    2. Introduction
    3. In Memoriam
    4. Research Articles
    5. Research Reviews
    6. Research Articles
    7. Clinical Reports
    8. Research Articles
    9. Clinical Reports
    10. Research Reviews
    11. New Syndrome
    12. Research Reviews
    1. Looking different: Understanding diversity in facial form (pages 2521–2529)

      S.A. Brugmann, J. Kim and J.A. Helms

      Version of Record online: 12 JUL 2006 | DOI: 10.1002/ajmg.a.31361

  4. Research Reviews

    1. Top of page
    2. Introduction
    3. In Memoriam
    4. Research Articles
    5. Research Reviews
    6. Research Articles
    7. Clinical Reports
    8. Research Articles
    9. Clinical Reports
    10. Research Reviews
    11. New Syndrome
    12. Research Reviews
    1. Molecular basis of human dentin diseases (pages 2536–2546)

      Mary MacDougall, Juan Dong and Ana Carolina Acevedo

      Version of Record online: 5 SEP 2006 | DOI: 10.1002/ajmg.a.31359

  5. Research Articles

    1. Top of page
    2. Introduction
    3. In Memoriam
    4. Research Articles
    5. Research Reviews
    6. Research Articles
    7. Clinical Reports
    8. Research Articles
    9. Clinical Reports
    10. Research Reviews
    11. New Syndrome
    12. Research Reviews
    1. Craniofacial and dental phenotype of Smith–Magenis syndrome (pages 2556–2561)

      Natalia Tomona, Ann C.M. Smith, Jean Pierre Guadagnini and Thomas C. Hart

      Version of Record online: 25 SEP 2006 | DOI: 10.1002/ajmg.a.31371

    2. PVRL1 variants contribute to non-syndromic cleft lip and palate in multiple populations (pages 2562–2570)

      Joseph R. Avila, Peter A. Jezewski, Alexandre R. Vieira, Iêda M. Orioli, Eduardo E. Castilla, Kaare Christensen, Sandra Daack-Hirsch, Paul A. Romitti and Jeffrey C. Murray

      Version of Record online: 6 NOV 2006 | DOI: 10.1002/ajmg.a.31367

    3. GLI2 mutations in four Brazilian patients: How wide is the phenotypic spectrum? (pages 2571–2576)

      Fedik Rahimov, Lucilene Arilho Ribeiro, Eziquiel de Miranda, Antonio Richieri-Costa and Jeffrey C. Murray

      Version of Record online: 9 NOV 2006 | DOI: 10.1002/ajmg.a.31370

    4. SIX3 mutations with holoprosencephaly (pages 2577–2583)

      Lucilene Arilho Ribeiro, Kenia B. El-Jaick, Maximilian Muenke and Antonio Richieri-Costa

      Version of Record online: 25 SEP 2006 | DOI: 10.1002/ajmg.a.31377

    5. Holoprosencephaly-like phenotype: Clinical and genetic perspectives (pages 2587–2593)

      A. Richieri-Costa and Lucilene Arilho Ribeiro

      Version of Record online: 25 SEP 2006 | DOI: 10.1002/ajmg.a.31378

  6. Clinical Reports

    1. Top of page
    2. Introduction
    3. In Memoriam
    4. Research Articles
    5. Research Reviews
    6. Research Articles
    7. Clinical Reports
    8. Research Articles
    9. Clinical Reports
    10. Research Reviews
    11. New Syndrome
    12. Research Reviews
    1. Contiguous gene syndrome of holoprosencephaly and hypotrichosis simplex: Association with an 18p11.3 deletion (pages 2598–2602)

      Piranit N. Kantaputra, Chanin Limwongse, Chintana Tochareontanaphol, Apiwat Mutirangura, Umnat Mevatee and Verayuth Praphanphoj

      Version of Record online: 25 SEP 2006 | DOI: 10.1002/ajmg.a.31386

  7. Research Articles

    1. Top of page
    2. Introduction
    3. In Memoriam
    4. Research Articles
    5. Research Reviews
    6. Research Articles
    7. Clinical Reports
    8. Research Articles
    9. Clinical Reports
    10. Research Reviews
    11. New Syndrome
    12. Research Reviews
  8. Clinical Reports

    1. Top of page
    2. Introduction
    3. In Memoriam
    4. Research Articles
    5. Research Reviews
    6. Research Articles
    7. Clinical Reports
    8. Research Articles
    9. Clinical Reports
    10. Research Reviews
    11. New Syndrome
    12. Research Reviews
    1. Patched mutations and hairy skin patches: A new sign in Gorlin syndrome (pages 2625–2630)

      Louise C. Wilson, Ekundayo Ajayi-Obe, Birgitta Bernhard and Saskia M. Maas

      Version of Record online: 11 AUG 2006 | DOI: 10.1002/ajmg.a.31374

  9. Research Reviews

    1. Top of page
    2. Introduction
    3. In Memoriam
    4. Research Articles
    5. Research Reviews
    6. Research Articles
    7. Clinical Reports
    8. Research Articles
    9. Clinical Reports
    10. Research Reviews
    11. New Syndrome
    12. Research Reviews
    1. Clinical dividends from the molecular genetic diagnosis of craniosynostosis (pages 2631–2639)

      Andrew O.M. Wilkie, Elena G. Bochukova, Ruth M. S. Hansen, Indira B. Taylor, Sahan V. Rannan-Eliya, Jo C. Byren, Steven A. Wall, Lina Ramos, Margarida Venâncio, Jane A. Hurst, Anthony W. O'Rourke, Louise J. Williams, Anneke Seller and Tracy Lester

      Version of Record online: 12 JUL 2006 | DOI: 10.1002/ajmg.a.31366

  10. New Syndrome

    1. Top of page
    2. Introduction
    3. In Memoriam
    4. Research Articles
    5. Research Reviews
    6. Research Articles
    7. Clinical Reports
    8. Research Articles
    9. Clinical Reports
    10. Research Reviews
    11. New Syndrome
    12. Research Reviews
    1. You have free access to this content
      A newly recognized polyosteolysis/hyperostosis syndrome (pages 2640–2645)

      Piranit N. Kantaputra, Chanin Limwongse, Ajchara Koolvisoot, Apichart Ausawamongkolkul and Somsiri Tayavitit

      Version of Record online: 25 SEP 2006 | DOI: 10.1002/ajmg.a.31373

  11. Research Reviews

    1. Top of page
    2. Introduction
    3. In Memoriam
    4. Research Articles
    5. Research Reviews
    6. Research Articles
    7. Clinical Reports
    8. Research Articles
    9. Clinical Reports
    10. Research Reviews
    11. New Syndrome
    12. Research Reviews

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