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There are 11930 results for: content related to: Analysis of ASPM in an ethnically diverse cohort of 400 patient samples: perspectives of the molecular diagnostic laboratory

  1. Genetic heterogeneity in Pakistani microcephaly families

    Clinical Genetics

    Volume 83, Issue 5, May 2013, Pages: 446–451, M Sajid Hussain, S Marriam Bakhtiar, M Farooq, I Anjum, E Janzen, M Reza Toliat, H Eiberg, KW Kjaer, N Tommerup, AA Noegel, P Nürnberg, SM Baig and L Hansen

    Version of Record online : 7 AUG 2012, DOI: 10.1111/j.1399-0004.2012.01932.x

  2. Genetic analysis of primary microcephaly in Indian families: novel ASPM mutations

    Clinical Genetics

    Volume 66, Issue 4, October 2004, Pages: 341–348, A Kumar, SH Blanton, M Babu, M Markandaya and SC Girimaji

    Version of Record online : 24 AUG 2004, DOI: 10.1111/j.1399-0004.2004.00304.x



    Volume 66, Issue 3, March 2012, Pages: 927–932, Stephen H. Montgomery and Nicholas I. Mundy

    Version of Record online : 1 DEC 2011, DOI: 10.1111/j.1558-5646.2011.01487.x

  4. Cerebral Cortex Evolution and the ASPM Gene

    Standard Article


    Farhan Ali

    Published Online : 15 SEP 2009, DOI: 10.1002/9780470015902.a0021765

  5. Compound heterozygous ASPM mutations in Pakistani MCPH families

    American Journal of Medical Genetics Part A

    Volume 149A, Issue 5, May 2009, Pages: 926–930, Farooq Muhammad, Shahid Mahmood Baig, Lars Hansen, Muhammad Sajid Hussain, Iram Anjum Inayat, Muhammad Aslam, Javed Anver Qureshi, Muhammad Toilat, Elisabeth Kirst, Muhammad Wajid, Peter Nürnberg, Hans Eiberg, Niels Tommerup and Klaus W. Kjaer

    Version of Record online : 7 APR 2009, DOI: 10.1002/ajmg.a.32749

  6. You have free access to this content
    Genetic, physiologic and ecogeographic factors contributing to variation in Homo sapiens: Homo floresiensis reconsidered

    Journal of Evolutionary Biology

    Volume 19, Issue 6, November 2006, Pages: 1744–1767, GARY D. RICHARDS

    Version of Record online : 21 JUN 2006, DOI: 10.1111/j.1420-9101.2006.01179.x

  7. Genetic causes of MCPH in consanguineous Pakistani families

    Clinical Genetics

    Volume 89, Issue 6, June 2016, Pages: 744–745, Nadine Kraemer, Sylvie Picker-Minh, Ansar A. Abbasi, Sebastian Fröhler, Olaf Ninnemann, Muhammad N. Khan, Ghazanfar Ali, Wei Chen and Angela M. Kaindl

    Version of Record online : 8 NOV 2015, DOI: 10.1111/cge.12685

  8. You have full text access to this OnlineOpen article
    Genome-wide analysis of the oxyntic proliferative isthmus zone reveals ASPM as a possible gastric stem/progenitor cell marker over-expressed in cancer

    The Journal of Pathology

    Volume 237, Issue 4, December 2015, Pages: 447–459, Pål Vange, Torunn Bruland, Vidar Beisvag, Sten Even Erlandsen, Arnar Flatberg, Berit Doseth, Arne K Sandvik and Ingunn Bakke

    Version of Record online : 26 AUG 2015, DOI: 10.1002/path.4591

  9. Primary microcephaly with ASPM mutation shows simplified cortical gyration with antero-posterior gradient pre- and post-natally

    American Journal of Medical Genetics Part A

    Volume 146A, Issue 11, 1 June 2008, Pages: 1439–1443, Julie Desir, Marie Cassart, Philippe David, Patrick Van Bogaert and Marc Abramowicz

    Version of Record online : 1 MAY 2008, DOI: 10.1002/ajmg.a.32312

  10. WDR62 missense mutation in a consanguineous family with primary microcephaly

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 3, March 2012, Pages: 622–625, Carlos A. Bacino, Luis A. Arriola, Joanna Wiszniewska and Penelope E. Bonnen

    Version of Record online : 3 FEB 2012, DOI: 10.1002/ajmg.a.34417

  11. Investigation of primary microcephaly in Bushehr province of Iran: novel STIL and ASPM mutations

    Clinical Genetics

    Volume 83, Issue 5, May 2013, Pages: 488–490, E Papari, M Bastami, A Farhadi, SS Abedini, M Hosseini, I Bahman, M Mohseni, M Garshasbi, L Abbasi Moheb, F Behjati, K Kahrizi, H-H Ropers and H Najmabadi

    Version of Record online : 18 SEP 2012, DOI: 10.1111/j.1399-0004.2012.01949.x

  12. You have full text access to this Open Access content
    Evidence for a second gene for primary microcephaly at MCPH5 on chromosome 1


    Volume 139, Issue 1, September 2003, Pages: 64–67, OLA WALLERMAN, AGNIES VAN EEGHEN, LEO P. TEN KATE and CLAES WADELIUS

    Version of Record online : 27 NOV 2003, DOI: 10.1111/j.1601-5223.2003.01682.x

  13. Absence of microcephalin gene mutations in a large cohort of non-consanguineous patients with autosomal recessive primary microcephaly

    American Journal of Medical Genetics Part A

    Volume 152A, Issue 11, November 2010, Pages: 2882–2885, Iris Scala, Luigi Titomanlio, Ennio Del Giudice, Sandrine Passemard, Chiara Figliuolo, Patrizia Annunziata, Barbara Granese, Elena Scarpato, Alain Verloes and Generoso Andria

    Version of Record online : 14 OCT 2010, DOI: 10.1002/ajmg.a.33672

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    Observations of the sensitivity of beam attenuation to particle size in a coastal bottom boundary layer

    Journal of Geophysical Research: Oceans (1978–2012)

    Volume 116, Issue C2, February 2011, P. S. Hill, E. Boss, J. P. Newgard, B. A. Law and T. G. Milligan

    Version of Record online : 16 FEB 2011, DOI: 10.1029/2010JC006539

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    Efficient insertional mutagenesis in rice using the maize En/Spm elements

    The Plant Journal

    Volume 44, Issue 5, December 2005, Pages: 879–892, Chellian Santhosh Kumar, Rod A. Wing and Venkatesan Sundaresan

    Version of Record online : 21 OCT 2005, DOI: 10.1111/j.1365-313X.2005.02570.x

  16. Severe presentation of WDR62 mutation: Is there a role for modifying genetic factors?

    American Journal of Medical Genetics Part A

    Volume 164, Issue 9, September 2014, Pages: 2161–2171, Cathryn J. Poulton, Rachel Schot, Katja Seufert, Maarten H. Lequin, Andrea Accogli, Giuseppe D' Annunzio, Laurent Villard, Nicole Philip, René de Coo, Coriene Catsman-Berrevoets, Ute Grasshoff, Anja Kattentidt-Mouravieva, Hans Calf, Erika de Vreugt-Gronloh, Leontine van Unen, Frans W. Verheijen, Niels Galjart, Deborah J. Morris-Rosendahl and Grazia M. S. Mancini

    Version of Record online : 19 MAY 2014, DOI: 10.1002/ajmg.a.36611

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    Hypoxia Enhances Tumor Stemness by Increasing the Invasive and Tumorigenic Side Population Fraction


    Volume 26, Issue 7, July 2008, Pages: 1818–1830, Bikul Das, Rika Tsuchida, David Malkin, Gideon Koren, Sylvain Baruchel and Herman Yeger

    Version of Record online : 8 MAY 2008, DOI: 10.1634/stemcells.2007-0724

  18. You have full text access to this Open Access content
    Evolution of man in the light of molecular genetics: a review. Part II. Regulation of gene function, evolution of speech and of brains


    Volume 145, Issue 3, June 2008, Pages: 113–125, Petter Portin

    Version of Record online : 27 MAY 2008, DOI: 10.1111/j.0018-0661.2008.02053.x

  19. Genetic causes of microcephaly and lessons for neuronal development

    Wiley Interdisciplinary Reviews: Developmental Biology

    Volume 2, Issue 4, July/August 2013, Pages: 461–478, Edward C. Gilmore and Christopher A. Walsh

    Version of Record online : 4 OCT 2012, DOI: 10.1002/wdev.89

  20. You have free access to this content


    Volume 63, Issue 10, October 2009, Pages: 2487–2490, Rasmus Nielsen

    Version of Record online : 10 SEP 2009, DOI: 10.1111/j.1558-5646.2009.00799.x