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There are 32377 results for: content related to: The developmental genetics of Hirschsprung's disease

  1. Building a brain in the gut: development of the enteric nervous system

    Clinical Genetics

    Volume 83, Issue 4, April 2013, Pages: 307–316, AM Goldstein, RMW Hofstra and AJ Burns

    Article first published online : 27 NOV 2012, DOI: 10.1111/cge.12054

  2. Re–Os and U–Pb Geochronology of the Dawan Mo–Zn–Fe Deposit in Northern Taihang Mountains, China

    Resource Geology

    Volume 64, Issue 2, April 2014, Pages: 117–135, Yang Song, Hai-Yang Ding, Xiao-Ming Qu, Rui-Jiang Wang, Wei Zhou and Shu-Zhi Wang

    Article first published online : 27 MAR 2014, DOI: 10.1111/rge.12032

  3. A cohort study of MFN2 mutations and phenotypic spectrums in Charcot–Marie–Tooth disease 2A patients

    Clinical Genetics

    B.-O. Choi, K. Nakhro, H.J. Park, Y.S. Hyun, J.H. Lee, S. Kanwal, S.-C. Jung and K.W. Chung

    Article first published online : 18 JUN 2014, DOI: 10.1111/cge.12432

  4. New insights into polar overdominance in callipyge sheep

    Animal Genetics

    Volume 45, Issue s1, August 2014, Pages: 51–61, C. A. Bidwell, J. N. Waddell, T. M. Taxis, H. Yu, R. L. Tellam, M. K. Neary and N. E. Cockett

    Article first published online : 2 JUL 2014, DOI: 10.1111/age.12132

  5. The Topological Multiplicities of Power: The Limits of Governing the Olympics

    Economic Geography

    Volume 90, Issue 3, July 2014, Pages: 321–339, Martin Müller

    Article first published online : 7 JAN 2014, DOI: 10.1111/ecge.12032

  6. Stated and Inferred Attribute Attendance Models: A Comparison with Environmental Choice Experiments

    Journal of Agricultural Economics

    Volume 64, Issue 3, September 2013, Pages: 719–736, Marit E. Kragt

    Article first published online : 19 AUG 2013, DOI: 10.1111/1477-9552.12032

  7. Transcriptional profiling and miRNA-dependent regulatory network analysis of longissimus dorsi muscle during prenatal and adult stages in two distinct pig breeds

    Animal Genetics

    Volume 44, Issue 4, August 2013, Pages: 398–407, P. Siengdee, N. Trakooljul, E. Murani, M. Schwerin, K. Wimmers and S. Ponsuksili

    Article first published online : 19 MAR 2013, DOI: 10.1111/age.12032

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    DFNB16 is a frequent cause of congenital hearing impairment: implementation of STRC mutation analysis in routine diagnostics

    Clinical Genetics

    B. Vona, M.A.H. Hofrichter, C. Neuner, J. Schröder, A. Gehrig, J.B. Hennermann, F. Kraus, W. Shehata-Dieler, E. Klopocki, I. Nanda and T. Haaf

    Article first published online : 21 JAN 2014, DOI: 10.1111/cge.12332

  9. Making headway with genetic diagnostics of intellectual disabilities

    Clinical Genetics

    Volume 85, Issue 2, February 2014, Pages: 101–110, M.H. Willemsen and T. Kleefstra

    Article first published online : 25 AUG 2013, DOI: 10.1111/cge.12244

  10. High incidence of large deletions in the PMS2 gene in Spanish Lynch syndrome families

    Clinical Genetics

    Volume 85, Issue 6, June 2014, Pages: 583–588, A.J. Brea-Fernández, J.M. Cameselle-Teijeiro, C. Alenda, C. Fernández-Rozadilla, J. Cubiella, J. Clofent, J.M. Reñé, U. Anido, M. Milá, F. Balaguer, A. Castells, S. Castellvi-Bel, R. Jover, A. Carracedo and C. Ruiz-Ponte

    Article first published online : 28 JUL 2013, DOI: 10.1111/cge.12232

  11. Epigenetic changes in diabetes

    Clinical Genetics

    Volume 84, Issue 1, July 2013, Pages: 1–10, ST Keating and A El-Osta

    Article first published online : 11 MAR 2013, DOI: 10.1111/cge.12121

  12. Epigenetic mechanisms in the pathogenesis of Lynch syndrome

    Clinical Genetics

    Volume 85, Issue 5, May 2014, Pages: 403–412, P. Peltomäki

    Article first published online : 17 FEB 2014, DOI: 10.1111/cge.12349

  13. The genetics of type 2 diabetes and its clinical relevance

    Clinical Genetics

    Volume 83, Issue 4, April 2013, Pages: 297–306, A Pal and MI McCarthy

    Article first published online : 4 DEC 2012, DOI: 10.1111/cge.12055

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    The classification and diagnostic algorithm for primary lymphatic dysplasia: an update from 2010 to include molecular findings

    Clinical Genetics

    Volume 84, Issue 4, October 2013, Pages: 303–314, FC Connell, K Gordon, G Brice, V Keeley, S Jeffery, PS Mortimer, S Mansour and P Ostergaard

    Article first published online : 27 JUN 2013, DOI: 10.1111/cge.12173

  15. Human facial dysostoses

    Clinical Genetics

    Volume 83, Issue 6, June 2013, Pages: 499–510, D Wieczorek

    Article first published online : 8 APR 2013, DOI: 10.1111/cge.12123

  16. Unmasking Kabuki syndrome

    Clinical Genetics

    Volume 83, Issue 3, March 2013, Pages: 201–211, N Bögershausen and B Wollnik

    Article first published online : 26 NOV 2012, DOI: 10.1111/cge.12051

  17. Cardiovascular manifestations in Marfan syndrome and related diseases; multiple genes causing similar phenotypes

    Clinical Genetics

    J.R. Cook, L. Carta, J. Galatioto and F. Ramirez

    Article first published online : 10 JUL 2014, DOI: 10.1111/cge.12436

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    The impact of next generation sequencing on the analysis of breast cancer susceptibility: a role for extremely rare genetic variation?

    Clinical Genetics

    Volume 84, Issue 5, November 2013, Pages: 407–414, FSM Hilbers, MPG Vreeswijk, CJ van Asperen and P Devilee

    Article first published online : 12 SEP 2013, DOI: 10.1111/cge.12256

  19. Charcot–Marie–Tooth disease and pathways to molecular based therapies

    Clinical Genetics

    T. Harel and J.R. Lupski

    Article first published online : 9 MAY 2014, DOI: 10.1111/cge.12393

  20. You have free access to this content
    Genetics of the corneal endothelial dystrophies: an evidence-based review

    Clinical Genetics

    Volume 84, Issue 2, August 2013, Pages: 109–119, A J Aldave, J Han and R F Frausto

    Article first published online : 10 JUN 2013, DOI: 10.1111/cge.12191