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There are 8415 results for: content related to: Non-genetic risk factors for holoprosencephaly

  1. Clinical epidemiologic study of holoprosencephaly in South America

    American Journal of Medical Genetics Part A

    Volume 143A, Issue 24, 15 December 2007, Pages: 3088–3099, Iêda M. Orioli and Eduardo E. Castilla

    Version of Record online : 6 NOV 2007, DOI: 10.1002/ajmg.a.32104

  2. Risk factors for nonsyndromic holoprosencephaly: A Manitoba case–control study

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 4, April 2012, Pages: 751–758, Simone S. Vaz, Bernard Chodirker, Chitra Prasad, Jamie A. Seabrook, Albert E. Chudley and Asuri N. Prasad

    Version of Record online : 14 MAR 2012, DOI: 10.1002/ajmg.a.35240

  3. Epidemiology of holoprosencephaly: Prevalence and risk factors

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

    Volume 154C, Issue 1, 15 February 2010, Pages: 13–21, Iêda M. Orioli and Eduardo E. Castilla

    Version of Record online : 26 JAN 2010, DOI: 10.1002/ajmg.c.30233

  4. A retrospective survey of perinatal risk factors of 104 living children with holoprosencephaly

    American Journal of Medical Genetics Part A

    Volume 128A, Issue 2, 15 July 2004, Pages: 114–119, Elaine E. Stashinko, Nancy J. Clegg, Heather A. Kammann, Vicki T. Sweet, Mauricio R. Delgado, Jin S. Hahn and Eric B. Levey

    Version of Record online : 23 MAR 2004, DOI: 10.1002/ajmg.a.30070

  5. Management of children with holoprosencephaly

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

    Volume 154C, Issue 1, 15 February 2010, Pages: 183–190, Eric B. Levey, Elaine Stashinko, Nancy J. Clegg and Mauricio R. Delgado

    Version of Record online : 26 JAN 2010, DOI: 10.1002/ajmg.c.30254

  6. Holoprosencephaly: signaling interactions between the brain and the face, the environment and the genes, and the phenotypic variability in animal models and humans

    Wiley Interdisciplinary Reviews: Developmental Biology

    Volume 4, Issue 1, January/February 2015, Pages: 17–32, Anna Petryk, Daniel Graf and Ralph Marcucio

    Version of Record online : 22 OCT 2014, DOI: 10.1002/wdev.161

  7. Risk factors for non-syndromic holoprosencephaly in the National Birth Defects Prevention Study

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

    Volume 154C, Issue 1, 15 February 2010, Pages: 62–72, Eric A. Miller, Sonja A. Rasmussen, Anna Maria Siega-Riz, Jaime L. Frías and Margaret A. Honein

    Version of Record online : 26 JAN 2010, DOI: 10.1002/ajmg.c.30244

  8. Holoprosencephaly: An update on cytogenetic abnormalities

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

    Volume 154C, Issue 1, 15 February 2010, Pages: 86–92, Claude Bendavid, Valérie Dupé, Lucie Rochard, Isabelle Gicquel, Christèle Dubourg and Véronique David

    Version of Record online : 26 JAN 2010, DOI: 10.1002/ajmg.c.30250

  9. Holoprosencephaly and agnathia spectrum: Presentation of two new patients and review of the literature

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

    Volume 154C, Issue 1, 15 February 2010, 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

    Version of Record online : 26 JAN 2010, DOI: 10.1002/ajmg.c.30235

  10. Neuroimaging advances in holoprosencephaly: Refining the spectrum of the midline malformation

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

    Volume 154C, Issue 1, 15 February 2010, Pages: 120–132, Jin S. Hahn and Patrick D. Barnes

    Version of Record online : 26 JAN 2010, DOI: 10.1002/ajmg.c.30238

  11. Potential synergistic effects of human placental extract and minoxidil on hair growth-promoting activity in C57BL/6J mice

    Clinical and Experimental Dermatology

    Volume 40, Issue 6, August 2015, Pages: 672–681, T.-R. Kwon, C. T. Oh, H. M. Park, H. J. Han, H. J. Ji and B. J. Kim

    Version of Record online : 18 MAR 2015, DOI: 10.1111/ced.12601

  12. The molecular genetics of holoprosencephaly

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

    Volume 154C, Issue 1, 15 February 2010, Pages: 52–61, Erich Roessler and Maximilian Muenke

    Version of Record online : 26 JAN 2010, DOI: 10.1002/ajmg.c.30236

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    A statistical downscaling to identify the large-scale circulation patterns associated with heavy precipitation events over southern France

    Quarterly Journal of the Royal Meteorological Society

    Volume 137, Issue 660, October 2011 Part A, Pages: 1812–1827, O. Nuissier, B. Joly, A. Joly, V. Ducrocq and P. Arbogast

    Version of Record online : 1 AUG 2011, DOI: 10.1002/qj.866

  14. Embryogenesis of holoprosencephaly

    American Journal of Medical Genetics Part A

    Volume 143A, Issue 24, 15 December 2007, Pages: 3079–3087, Kohei Shiota, Shigehito Yamada, Munekazu Komada and Makoto Ishibashi

    Version of Record online : 26 OCT 2007, DOI: 10.1002/ajmg.a.32020

  15. Current recommendations for the molecular evaluation of newly diagnosed holoprosencephaly patients

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

    Volume 154C, Issue 1, 15 February 2010, Pages: 93–101, Daniel E. Pineda-Alvarez, Christèle Dubourg, Véronique David, Erich Roessler and Maximilian Muenke

    Version of Record online : 26 JAN 2010, DOI: 10.1002/ajmg.c.30253

  16. Genetic counseling and “molecular” prenatal diagnosis of holoprosencephaly (HPE)

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

    Volume 154C, Issue 1, 15 February 2010, Pages: 191–196, Sandra Mercier, Christèle Dubourg, Marion Belleguic, Laurent Pasquier, Philippe Loget, Josette Lucas, Claude Bendavid and Sylvie Odent

    Version of Record online : 26 JAN 2010, DOI: 10.1002/ajmg.c.30246

  17. Analysis of genotype–phenotype correlations in human holoprosencephaly

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

    Volume 154C, Issue 1, 15 February 2010, 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

    Version of Record online : 26 JAN 2010, DOI: 10.1002/ajmg.c.30240

  18. Early pathogenesis of holoprosencephaly

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

    Volume 154C, Issue 1, 15 February 2010, Pages: 22–28, Kohei Shiota and Shigehito Yamada

    Version of Record online : 26 JAN 2010, DOI: 10.1002/ajmg.c.30248

  19. SHH mutation is associated with solitary median maxillary central incisor: A study of 13 patients and review of the literature

    American Journal of Medical Genetics

    Volume 102, Issue 1, 22 July 2001, Pages: 1–10, Luisa Nanni, Jeffrey E. Ming, Yangzhu Du, Roger K. Hall, Michael Aldred, Agnes Bankier and Maximilian Muenke

    Version of Record online : 5 JUL 2001, DOI: 10.1002/1096-8628(20010722)102:1<1::AID-AJMG1336>3.0.CO;2-U

  20. Single median maxillary central incisor: New data and mutation review

    Birth Defects Research Part A: Clinical and Molecular Teratology

    Volume 79, Issue 8, August 2007, Pages: 573–580, Kênia B. El-Jaick, Renata F. Fonseca, Miguel A. Moreira, Márcia G. Ribeiro, Ana M. Bolognese, Sânia O. Dias, Eliane T. Pereira, Eduardo E. Castilla and Iêda M. Orioli

    Version of Record online : 21 JUN 2007, DOI: 10.1002/bdra.20380