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There are 9158 results for: content related to: 1.15 Mb microdeletion in chromosome band 20p13 associated with moderate developmental delay—Additional case and data's review

  1. CGH arrays compared for DNA isolated from formalin-fixed, paraffin-embedded material

    Genes, Chromosomes and Cancer

    Volume 51, Issue 4, April 2012, Pages: 344–352, Oscar Krijgsman, Danielle Israeli, Josien C. Haan, Hendrik F. van Essen, Serge J. Smeets, Paul P. Eijk, Renske D. M. Steenbergen, Klaas Kok, Sabine Tejpar, Gerrit A. Meijer and Bauke Ylstra

    Version of Record online : 8 DEC 2011, DOI: 10.1002/gcc.21920

  2. You have full text access to this Open Access content
    Targeted re-sequencing of the allohexaploid wheat exome

    Plant Biotechnology Journal

    Volume 10, Issue 6, August 2012, Pages: 733–742, Mark O. Winfield, Paul A. Wilkinson, Alexandra M. Allen, Gary L. A. Barker, Jane A. Coghill, Amanda Burridge, Anthony Hall, Rachael C. Brenchley, Rosalinda D’Amore, Neil Hall, Michael W. Bevan, Todd Richmond, Daniel J. Gerhardt, Jeffrey A. Jeddeloh and Keith J. Edwards

    Version of Record online : 17 JUN 2012, DOI: 10.1111/j.1467-7652.2012.00713.x

  3. Overview of Target Enrichment Strategies


    Current Protocols in Molecular Biology


    Iwanka Kozarewa, Javier Armisen, Andrew F. Gardner, Barton E. Slatko and C.L. Hendrickson

    Published Online : 1 OCT 2015, DOI: 10.1002/0471142727.mb0721s112

  4. Assessing the Enrichment Performance in Targeted Resequencing Experiments

    Human Mutation

    Volume 33, Issue 4, April 2012, Pages: 635–641, Peter Frommolt, Ali T. Abdallah, Janine Altmüller, Susanne Motameny, Holger Thiele, Christian Becker, Kathryn Stemshorn, Matthias Fischer, Tobias Freilinger and Peter Nürnberg

    Version of Record online : 28 FEB 2012, DOI: 10.1002/humu.22036

  5. Candidate driver genes in focal chromosomal aberrations of stage II colon cancer

    The Journal of Pathology

    Volume 221, Issue 4, August 2010, Pages: 411–424, Rebecca PM Brosens, Josien C Haan, Beatriz Carvalho, François Rustenburg, Heike Grabsch, Philip Quirke, Alexander F Engel, Miguel A Cuesta, Nicola Maughan, Marcel Flens, Gerrit A Meijer and Bauke Ylstra

    Version of Record online : 23 APR 2010, DOI: 10.1002/path.2724

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    Detection of novel genetic variation in autosomal dominant retinitis pigmentosa

    Clinical Genetics

    Volume 84, Issue 5, November 2013, Pages: 441–452, E Borràs, M de Sousa Dias, I Hernan, B Pascual, B Mañé, MJ Gamundi, B Delás and M Carballo

    Version of Record online : 15 APR 2013, DOI: 10.1111/cge.12151

  7. A novel α0-thalassemia deletion in a Greek patient with HbH disease and β-thalassemia trait

    European Journal of Haematology

    Volume 88, Issue 4, April 2012, Pages: 356–362, Marion Phylipsen, Jan Traeger-Synodinos, Martijn van der Kraan, Peter van Delft, Greet Bakker, Mariska Geerts, Emmanuel Kanavakis, Alexandra Stamoulakatou, Markissia Karagiorga, Piero C. Giordano and Cornelis L. Harteveld

    Version of Record online : 11 FEB 2012, DOI: 10.1111/j.1600-0609.2012.01748.x

  8. Comprehensive High-Throughput Arrays for Relative Methylation (CHARM)


    Current Protocols in Human Genetics


    Christine Ladd-Acosta, Martin J. Aryee, Jared M. Ordway and Andrew P. Feinberg

    Published Online : 1 APR 2010, DOI: 10.1002/0471142905.hg2001s65

  9. Functional genomics of the brain: uncovering networks in the CNS using a systems approach

    Wiley Interdisciplinary Reviews: Systems Biology and Medicine

    Volume 3, Issue 6, November/December 2011, Pages: 628–648, Genevieve Konopka

    Version of Record online : 31 DEC 2010, DOI: 10.1002/wsbm.139

  10. You have full text access to this OnlineOpen article
    Using genic sequence capture in combination with a syntenic pseudo genome to map a deletion mutant in a wheat species

    The Plant Journal

    Volume 80, Issue 5, December 2014, Pages: 895–904, Laura-Jayne Gardiner, Piotr Gawroński, Lisa Olohan, Thorsten Schnurbusch, Neil Hall and Anthony Hall

    Version of Record online : 9 OCT 2014, DOI: 10.1111/tpj.12660

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    Next-generation sequencing for mitochondrial disorders

    British Journal of Pharmacology

    Volume 171, Issue 8, April 2014, Pages: 1837–1853, C J Carroll, V Brilhante and A Suomalainen

    Version of Record online : 28 MAR 2014, DOI: 10.1111/bph.12469

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    Repeat subtraction-mediated sequence capture from a complex genome

    The Plant Journal

    Volume 62, Issue 5, June 2010, Pages: 898–909, Yan Fu, Nathan M. Springer, Daniel J. Gerhardt, Kai Ying, Cheng-Ting Yeh, Wei Wu, Ruth Swanson-Wagner, Mark D’Ascenzo, Tracy Millard, Lindsay Freeberg, Natsuyo Aoyama, Jacob Kitzman, Daniel Burgess, Todd Richmond, Thomas J. Albert, W. Brad Barbazuk, Jeffrey A. Jeddeloh and Patrick S. Schnable

    Version of Record online : 4 MAR 2010, DOI: 10.1111/j.1365-313X.2010.04196.x

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    Whole exome sequencing is an efficient and sensitive method for detection of germline mutations in patients with phaeochromcytomas and paragangliomas

    Clinical Endocrinology

    Volume 80, Issue 1, January 2014, Pages: 25–33, Aideen M. McInerney-Leo, Mhairi S. Marshall, Brooke Gardiner, Diana E. Benn, Janelle McFarlane, Bruce G. Robinson, Matthew A. Brown, Paul J. Leo, Roderick J. Clifton-Bligh and Emma L. Duncan

    Version of Record online : 25 OCT 2013, DOI: 10.1111/cen.12331

  14. Candidate locus analysis for PHACE syndrome

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 6, June 2012, Pages: 1363–1367, Sheri Mitchell, Dawn H. Siegel, Joseph T.C. Shieh, David A. Stevenson, J. Fredrik Grimmer, Tracey Lewis, Denise Metry, Ilona Frieden, Francine Blei, Hulya Kayserili, Beth A. Drolet and Pinar Bayrak-Toydemir

    Version of Record online : 27 APR 2012, DOI: 10.1002/ajmg.a.35341

  15. Triplet-Sensitized Photodeprotection of Oligonucleotides in Solution and on Microarray Chips

    Helvetica Chimica Acta

    Volume 87, Issue 1, January 2004, Pages: 28–45, Dominik Wöll, Stefan Walbert, Klaus-Peter Stengele, Tom J. Albert, Todd Richmond, Jason Norton, Michael Singer, Roland D. Green, Wolfgang Pfleiderer and Ulrich E. Steiner

    Version of Record online : 2 FEB 2004, DOI: 10.1002/hlca.200490015

  16. Molecular cytogenetic characterization of the first reported case of inv dup del 20p compatible with a U-type exchange model

    American Journal of Medical Genetics Part A

    Volume 149A, Issue 3, March 2009, Pages: 437–445, Sandrine Leclercq, Kim Maincent, Françoise Baverel, Dominique Le Tessier, Franck Letourneur, Aziza Lebbar and Jean-Michel Dupont

    Version of Record online : 10 FEB 2009, DOI: 10.1002/ajmg.a.32640

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    Network analysis reveals the relationship among wood properties, gene expression levels and genotypes of natural Populus trichocarpa accessions

    New Phytologist

    Volume 200, Issue 3, November 2013, Pages: 727–742, Ilga Porth, Jaroslav Klápště, Oleksandr Skyba, Michael C. Friedmann, Jan Hannemann, Juergen Ehlting, Yousry A. El-Kassaby, Shawn D. Mansfield and Carl J. Douglas

    Version of Record online : 29 JUL 2013, DOI: 10.1111/nph.12419

  18. Validation of comparative genomic hybridization arrays for the detection of genomic rearrangements of the calpain-3 and dysferlin genes

    Clinical Genetics

    Volume 81, Issue 1, January 2012, Pages: 99–101, M Bartoli, P Nègre, N Wein, P Bourgeois, C Pécheux, N Lévy and Martin Krahn

    Version of Record online : 12 DEC 2011, DOI: 10.1111/j.1399-0004.2011.01708.x

  19. Genome-wide screening of aberrant DNA methylation which associated with gene expression in mouse skin cancers

    Molecular Carcinogenesis

    Volume 54, Issue 3, March 2015, Pages: 178–188, Kyoko Fujiwara, Srimoyee Ghosh, Ping Liang, Evan Morien, Masayoshi Soma and Hiroki Nagase

    Version of Record online : 24 SEP 2013, DOI: 10.1002/mc.22085

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    Biotech meetings, market and funding

    Biotechnology Journal

    Volume 3, Issue 5, May 2008, Pages: 583–589,

    Version of Record online : 15 MAY 2008, DOI: 10.1002/biot.200890052