Search Results

There are 7455 results for: content related to: Prevalence of autism according to maternal immigrant status and ethnic origin

  1. You have free access to this content
    Ethnic origin and increased risk for schizophrenia in immigrants to countries of recent and longstanding immigration

    Acta Psychiatrica Scandinavica

    Volume 121, Issue 5, May 2010, Pages: 325–339, M.-J. Dealberto

    Article first published online : 25 JAN 2010, DOI: 10.1111/j.1600-0447.2009.01535.x

  2. Vitamin D and maternal and child health: Overview and implications for dietary requirements

    Birth Defects Research Part C: Embryo Today: Reviews

    Volume 99, Issue 1, March 2013, Pages: 24–44, Janet Y. Uriu-Adams, Sarah G. Obican and Carl L. Keen

    Article first published online : 30 MAY 2013, DOI: 10.1002/bdrc.21031

  3. You have full text access to this OnlineOpen article
    Low maternal vitamin D status and fetal bone development: Cohort study

    Journal of Bone and Mineral Research

    Volume 25, Issue 1, January 2010, Pages: 14–19, Pamela Mahon, Nicholas Harvey, Sarah Crozier, Hazel Inskip, Sian Robinson, Nigel Arden, Rama Swaminathan, Cyrus Cooper and Keith Godfrey

    Article first published online : 14 DEC 2009, DOI: 10.1359/jbmr.090701

  4. Disciplinary Impact and Technological Obsolescence in Digital Medieval Studies1

    A Companion to Digital Literary Studies

    Ray Siemens, Susan Schreibman, Pages: 65–81, 2013

    Published Online : 4 OCT 2013, DOI: 10.1002/9781405177504.ch3

  5. Maternal Vitamin D Status as a Critical Determinant in Gestational Diabetes

    Journal of Obstetric, Gynecologic, & Neonatal Nursing

    Volume 41, Issue 3, May/June 2012, Pages: 328–338, Jeanine Senti, Doria K. Thiele and Cindy Miller Anderson

    Article first published online : 17 MAY 2012, DOI: 10.1111/j.1552-6909.2012.01366.x

  6. Imprinting Disorders

    Standard Article


    Rebecca S Henkhaus, Andrew P Feinberg, Emily L Niemitz and Merlin G Butler

    Published Online : 15 SEP 2011, DOI: 10.1002/9780470015902.a0005477.pub2

  7. Two Iranian families with a novel mutation in GJB2 causing autosomal dominant nonsyndromic hearing loss

    American Journal of Medical Genetics Part A

    Volume 155, Issue 5, May 2011, Pages: 1202–1211, Niloofar Bazazzadegan, Abraham M. Sheffield, Masoomeh Sobhani, Kimia Kahrizi, Nicole C. Meyer, Guy Van Camp, Nele Hilgert, Seyedeh Sedigheh Abedini, Farkhondeh Habibi, Ahmad Daneshi, Carla Nishimura, Matthew R. Avenarius, Mohammad Farhadi, Richard J.H. Smith and Hossein Najmabadi

    Article first published online : 11 APR 2011, DOI: 10.1002/ajmg.a.33209

  8. You have free access to this content
    NGOs, IOs, and the ICC: Diagnosing and Framing Darfur

    Sociological Forum

    Volume 29, Issue 1, March 2014, Pages: 29–51, Meghan Zacher, Hollie Nyseth Brehm and Joachim J. Savelsberg

    Article first published online : 8 JAN 2014, DOI: 10.1111/socf.12068

  9. Maternal vitamin D deficiency causes smaller muscle fibers and altered transcript levels of genes involved in protein degradation, myogenesis, and cytoskeleton organization in the newborn rat

    Molecular Nutrition & Food Research

    Volume 58, Issue 2, February 2014, Pages: 343–352, Daniela Max, Corinna Brandsch, Sarah Schumann, Hagen Kühne, Matthias Frommhagen, Alexandra Schutkowski, Frank Hirche, Martin S. Staege and Gabriele I. Stangl

    Article first published online : 21 AUG 2013, DOI: 10.1002/mnfr.201300360

  10. Gastric Cancer

    Standard Article


    Karl-Friedrich Becker and Gisela Keller

    Published Online : 18 OCT 2010, DOI: 10.1002/9780470015902.a0006056.pub2

  11. DNA Helicase-deficiency Disorders

    Standard Article


    Julia M Sidorova and Raymond J Monnat

    Published Online : 15 NOV 2010, DOI: 10.1002/9780470015902.a0006065.pub2

  12. Renal Carcinoma and von Hippel–Lindau Disease

    Standard Article


    Thomas M Connor and Patrick H Maxwell

    Published Online : 18 OCT 2010, DOI: 10.1002/9780470015902.a0006062.pub2

  13. Family studies of infantile visceral myopathy: A congenital myopathic pseudo-obstruction syndrome

    American Journal of Medical Genetics

    Volume 82, Issue 2, 15 January 1999, Pages: 114–122, Carol D. Guzé, Paul E. Hyman and Valerie J. Payne

    Article first published online : 29 JAN 1999, DOI: 10.1002/(SICI)1096-8628(19990115)82:2<114::AID-AJMG3>3.0.CO;2-H

  14. It's only teeth – are there limits to genetic testing?

    Clinical Genetics

    Volume 63, Issue 5, May 2003, Pages: 333–339, MJ Aldred, PJM Crawford, R Savarirayan and J Savulescu

    Article first published online : 7 MAY 2003, DOI: 10.1034/j.1399-0004.2003.00045.x

  15. Educational Ethnography and the Politics of Globalization, War, and Resistance

    Anthropology & Education Quarterly

    Volume 36, Issue 4, December 2005, Pages: 315–328, Pauline Lipman

    Article first published online : 8 JAN 2008, DOI: 10.1525/aeq.2005.36.4.315

  16. Consequences of cultural satisfaction at work: A study of New Zealand Māori

    Asia Pacific Journal of Human Resources

    Volume 49, Issue 4, December 2011, Pages: 461–475, Jarrod M Haar and David Brougham

    Article first published online : 30 DEC 2011, DOI: 10.1177/1038411111423477

  17. More than an open door: Deploying philanthropy to student access and success in American community colleges

    New Directions for Student Services

    Volume 2010, Issue 130, Summer 2010, Pages: 55–70, Joyce C. Romano, Geraldine Gallagher and Sanford C. Shugart

    Article first published online : 24 JUN 2010, DOI: 10.1002/ss.360

  18. Compartmentalization of the foregut tube: developmental origins of the trachea and esophagus

    Wiley Interdisciplinary Reviews: Developmental Biology

    Volume 1, Issue 2, March/April 2012, Pages: 184–202, Sarah R. Fausett and John Klingensmith

    Article first published online : 21 NOV 2011, DOI: 10.1002/wdev.12

  19. 18q- syndrome and ectodermal dysplasia syndrome: Description of a child and his family

    American Journal of Medical Genetics Part A

    Volume 116A, Issue 2, 15 January 2003, Pages: 192–199, R. Zannolli, M. Pierluigi, L. Pucci, N. Lagrasta, O. Gasparre, M.R. Matera, R.M. Di Bartolo, M.A. Mazzei, P. Sacco, C. Miracco, M.M. de Santi, P. Aitiani, S. Cavani, L. Pellegrini, M. Fimiani, C. Alessandrini, P. Galluzzi, W. Livi, S. Gonnelli, P. Terrosi-Vagnoli, M. Zappella and G. Morgese

    Article first published online : 19 DEC 2002, DOI: 10.1002/ajmg.a.10069

  20. Mutations of mitochondrial DNA polymerase γA are a frequent cause of autosomal dominant or recessive progressive external ophthalmoplegia

    Annals of Neurology

    Volume 52, Issue 2, August 2002, Pages: 211–219, Eleonora Lamantea, Valeria Tiranti, Andreina Bordoni, Antonio Toscano, Francesco Bono, Serena Servidei, Alex Papadimitriou, Hans Spelbrink, Laura Silvestri, Giorgio Casari, Giacomo P. Comi and Massimo Zeviani

    Article first published online : 21 JUN 2002, DOI: 10.1002/ana.10278