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

Cover image for Vol. 154C Issue 1

Special Issue: Holoprosencephaly

15 February 2010

Volume 154C, Issue 1

Pages 1–201

Issue edited by: Maximilian Muenke, Benjamin Solomon, Sylvie Odent

  1. Introduction

    1. Top of page
    2. Introduction
    3. Articles
    1. Introduction to the American Journal of Medical Genetics Part C on holoprosencephaly (pages 1–2)

      Maximilian Muenke, Benjamin D. Solomon and Sylvie Odent

      Article first published online: 26 JAN 2010 | DOI: 10.1002/ajmg.c.30255

  2. Articles

    1. Top of page
    2. Introduction
    3. Articles
    1. Holoprosencephaly flashcards: A summary for the clinician (pages 3–7)

      Benjamin D. Solomon, Daniel E. Pineda-Alvarez, Sandra Mercier, Manu S. Raam, Sylvie Odent and Maximilian Muenke

      Article first published online: 26 JAN 2010 | DOI: 10.1002/ajmg.c.30245

    2. Early pathogenesis of holoprosencephaly (pages 22–28)

      Kohei Shiota and Shigehito Yamada

      Article first published online: 26 JAN 2010 | DOI: 10.1002/ajmg.c.30248

    3. Genesis of teratogen-induced holoprosencephaly in mice (pages 29–42)

      Robert J. Lipinski, Elizabeth A. Godin, Shonagh K. O'leary-Moore, Scott E. Parnell and Kathleen K. Sulik

      Article first published online: 26 JAN 2010 | DOI: 10.1002/ajmg.c.30239

    4. Roles of bone morphogenetic protein signaling and its antagonism in holoprosencephaly (pages 43–51)

      John Klingensmith, Maiko Matsui, Yu-Ping Yang and Ryan M. Anderson

      Article first published online: 26 JAN 2010 | DOI: 10.1002/ajmg.c.30256

    5. The molecular genetics of holoprosencephaly (pages 52–61)

      Erich Roessler and Maximilian Muenke

      Article first published online: 26 JAN 2010 | DOI: 10.1002/ajmg.c.30236

    6. Risk factors for non-syndromic holoprosencephaly in the National Birth Defects Prevention Study (pages 62–72)

      Eric A. Miller, Sonja A. Rasmussen, Anna Maria Siega-Riz, Jaime L. Frías and Margaret A. Honein

      Article first published online: 26 JAN 2010 | DOI: 10.1002/ajmg.c.30244

    7. Non-genetic risk factors for holoprosencephaly (pages 73–85)

      Candice Y. Johnson and Sonja A. Rasmussen

      Article first published online: 26 JAN 2010 | DOI: 10.1002/ajmg.c.30242

    8. Holoprosencephaly: An update on cytogenetic abnormalities (pages 86–92)

      Claude Bendavid, Valérie Dupé, Lucie Rochard, Isabelle Gicquel, Christèle Dubourg and Véronique David

      Article first published online: 26 JAN 2010 | DOI: 10.1002/ajmg.c.30250

    9. Current recommendations for the molecular evaluation of newly diagnosed holoprosencephaly patients (pages 93–101)

      Daniel E. Pineda-Alvarez, Christèle Dubourg, Véronique David, Erich Roessler and Maximilian Muenke

      Article first published online: 26 JAN 2010 | DOI: 10.1002/ajmg.c.30253

    10. Neuropathology of holoprosencephaly (pages 109–119)

      Pascale Marcorelles and Annie Laquerriere

      Article first published online: 26 JAN 2010 | DOI: 10.1002/ajmg.c.30249

    11. Analysis of genotype–phenotype correlations in human holoprosencephaly (pages 133–141)

      Benjamin D. Solomon, Sandra Mercier, Jorge I. Vélez, Daniel E. Pineda-Alvarez, Adrian Wyllie, Nan Zhou, Christèle Dubourg, Veronique David, Sylvie Odent, Erich Roessler and Maximilian Muenke

      Article first published online: 26 JAN 2010 | DOI: 10.1002/ajmg.c.30240

    12. Cyclopia (synophthalmia) in Smith–Lemli–Opitz syndrome: First reported case and consideration of mechanism (pages 142–145)

      David D. Weaver, Benjamin D. Solomon, Kelly Akin-Samson, Richard I. Kelley and Maximilian Muenke

      Article first published online: 26 JAN 2010 | DOI: 10.1002/ajmg.c.30241

    13. Holoprosencephaly due to numeric chromosome abnormalities (pages 146–148)

      Benjamin D. Solomon, Kenneth N. Rosenbaum, Jeanne M. Meck and Maximilian Muenke

      Article first published online: 26 JAN 2010 | DOI: 10.1002/ajmg.c.30232

    14. Holoprosencephaly and agnathia spectrum: Presentation of two new patients and review of the literature (pages 158–169)

      Emily F. Kauvar, Benjamin D. Solomon, Cynthia J.R. Curry, Anthonie J. van Essen, Nicole Janssen, Amalia Dutra, Erich Roessler and Maximilian Muenke

      Article first published online: 26 JAN 2010 | DOI: 10.1002/ajmg.c.30235

    15. Holoprosencephaly and ectrodactyly: Report of three new patients and review of the literature (pages 170–175)

      Amelia A. Keaton, Benjamin D. Solomon, Anthonie J. van Essen, Kathleen M. Pfleghaar, Michael A. Slama, Judith A. Martin and Maximilian Muenke

      Article first published online: 26 JAN 2010 | DOI: 10.1002/ajmg.c.30251

    16. Holoprosencephaly and craniosynostosis: A report of two siblings and review of the literature (pages 176–182)

      Manu S. Raam, Benjamin D. Solomon, Stavit A. Shalev and Maximilian Muenke

      Article first published online: 26 JAN 2010 | DOI: 10.1002/ajmg.c.30234

    17. Management of children with holoprosencephaly (pages 183–190)

      Eric B. Levey, Elaine Stashinko, Nancy J. Clegg and Mauricio R. Delgado

      Article first published online: 26 JAN 2010 | DOI: 10.1002/ajmg.c.30254

    18. Genetic counseling and “molecular” prenatal diagnosis of holoprosencephaly (HPE) (pages 191–196)

      Sandra Mercier, Christèle Dubourg, Marion Belleguic, Laurent Pasquier, Philippe Loget, Josette Lucas, Claude Bendavid and Sylvie Odent

      Article first published online: 26 JAN 2010 | DOI: 10.1002/ajmg.c.30246

    19. Parental perspectives on living with a child with HoPE (pages 197–201)

      Elaine E. Stashinko, Leslie A. Harley, Roxanne A. Steele and Nancy J. Clegg

      Article first published online: 26 JAN 2010 | DOI: 10.1002/ajmg.c.30237

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