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There are 127918 results for: content related to: Prevalence of autism according to maternal immigrant status and ethnic origin

  1. 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

  2. Vitamin D bioavailability in cystic fibrosis: a cause for concern?

    Nutrition Reviews

    Volume 70, Issue 5, May 2012, Pages: 280–293, Geneviève Mailhot

    Article first published online : 30 MAR 2012, DOI: 10.1111/j.1753-4887.2012.00471.x

  3. Linking genotypes, phenotypes, and fitness in wild primate populations

    Evolutionary Anthropology: Issues, News, and Reviews

    Volume 20, Issue 3, May/June 2011, Pages: 104–119, Brenda J. Bradley and Richard R. Lawler

    Article first published online : 22 JUN 2011, DOI: 10.1002/evan.20306

  4. High hyperdiploid childhood acute lymphoblastic leukemia

    Genes, Chromosomes and Cancer

    Volume 48, Issue 8, August 2009, Pages: 637–660, Kajsa Paulsson and Bertil Johansson

    Article first published online : 4 MAY 2009, DOI: 10.1002/gcc.20671

  5. Hypoglycemia: Assessment and Management

    Brook's Clinical Pediatric Endocrinology, Sixth Edition

    Andrew Cotterill, David Cowley, Ristan Greer, Pages: 505–529, 2010

    Published Online : 20 JUN 2010, DOI: 10.1002/9781444316728.ch19

  6. You have free access to this content
    The genetics of hereditary melanoma and nevi


    Volume 86, Issue S11, 1 December 1999, Pages: 2464–2477, Mark H. Greene

    Article first published online : 20 NOV 2000, DOI: 10.1002/(SICI)1097-0142(19991201)86:11+<2464::AID-CNCR3>3.0.CO;2-F

  7. Diseases of the tooth: the genetic and molecular basis of inherited anomalies affecting the dentition

    Wiley Interdisciplinary Reviews: Developmental Biology

    Volume 2, Issue 2, March/April 2013, Pages: 183–212, Martyn T. Cobourne and Paul T. Sharpe

    Article first published online : 25 MAY 2012, DOI: 10.1002/wdev.66

  8. Revealing the human mutome

    Clinical Genetics

    Volume 78, Issue 4, October 2010, Pages: 310–320, JM Chen, C Férec and DN Cooper

    Article first published online : 22 MAY 2010, DOI: 10.1111/j.1399-0004.2010.01474.x

  9. Identical but not the same: The value of discordant monozygotic twins in genetic research

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 153B, Issue 6, September 2010, Pages: 1134–1149, Petra J.G. Zwijnenburg, Hanne Meijers-Heijboer and Dorret I. Boomsma

    Article first published online : 28 APR 2010, DOI: 10.1002/ajmg.b.31091

  10. The molecular basis of human congenital limb malformations

    Wiley Interdisciplinary Reviews: Developmental Biology

    Volume 1, Issue 6, November/December 2012, Pages: 803–822, Aimée Zuniga, Rolf Zeller and Simone Probst

    Article first published online : 26 APR 2012, DOI: 10.1002/wdev.59

  11. Chapter 88. Sclerosing Bone Disorders

    Primer on the Metabolic Bone Diseases and Disorders of Mineral Metabolism

    , Pages: 411–423, 2009

    Published Online : 23 DEC 2009, DOI: 10.1002/9780470623992.ch88

  12. Synteny-defined candidate genes for congenital and idiopathic scoliosis

    American Journal of Medical Genetics

    Volume 83, Issue 3, 19 March 1999, Pages: 164–177, Philip F. Giampietro, Cathleen L. Raggio and Robert D. Blank

    Article first published online : 4 MAR 1999, DOI: 10.1002/(SICI)1096-8628(19990319)83:3<164::AID-AJMG5>3.0.CO;2-D

  13. Biochemie und Molekulargenetik 2000

    Nachrichten aus der Chemie

    Volume 49, Issue 3, März 2001, Pages: 321–336, Brunhilde Wirth, Stefan Zwilling, Hermann Lübbert, Thomas Herget, Christian Behl and Bernd Moosmann

    Article first published online : 1 MAY 2010, DOI: 10.1002/nadc.20010490309

  14. Huntington's Disease

    Neurodegeneration: The Molecular Pathology of Dementia and Movement Disorders, Second Edition

    John C. Hedreen, Raymund A. C. Roos, Pages: 258–272, 2011

    Published Online : 21 SEP 2011, DOI: 10.1002/9781444341256.ch26

  15. Review of the Lynch syndrome: history, molecular genetics, screening, differential diagnosis, and medicolegal ramifications

    Clinical Genetics

    Volume 76, Issue 1, July 2009, Pages: 1–18, HT Lynch, PM Lynch, SJ Lanspa, CL Snyder, JF Lynch and CR Boland

    Article first published online : 15 JUL 2009, DOI: 10.1111/j.1399-0004.2009.01230.x

  16. Changing clinicopathological practice in parathyroid disease


    Volume 56, Issue 7, June 2010, Pages: 835–851, Sarah J Johnson

    Article first published online : 18 MAY 2010, DOI: 10.1111/j.1365-2559.2010.03515.x

  17. X-linked mental retardation: vanishing boundaries between non-specific (MRX) and syndromic (MRXS) forms

    Clinical Genetics

    Volume 62, Issue 6, December 2002, Pages: 423–432, SGM Frints, G Froyen, P Marynen and J-P Fryns

    Article first published online : 13 DEC 2002, DOI: 10.1034/j.1399-0004.2002.620601.x

  18. Vitamin D inadequacy in pregnancy: biology, outcomes, and interventions

    Nutrition Reviews

    Volume 68, Issue 8, August 2010, Pages: 465–477, Daphna K Dror and Lindsay H Allen

    Article first published online : 20 JUL 2010, DOI: 10.1111/j.1753-4887.2010.00306.x

  19. You have full text access to this Open Access content
    Caveolins in rhabdomyosarcoma

    Journal of Cellular and Molecular Medicine

    Volume 15, Issue 12, December 2011, Pages: 2553–2568, Stefania Rossi, Pietro Luigi Poliani, Cristina Missale, Eugenio Monti and Alessandro Fanzani

    Article first published online : 28 NOV 2011, DOI: 10.1111/j.1582-4934.2011.01364.x

  20. The epidemiology of mental retardation: Challenges and opportunities in the new millennium

    Mental Retardation and Developmental Disabilities Research Reviews

    Volume 8, Issue 3, 2002, Pages: 117–134, Helen Leonard and Xingyan Wen

    Article first published online : 4 SEP 2002, DOI: 10.1002/mrdd.10031