Canlyniadau Chwilio - Jeroen Knijnenburg

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  1. 1
    Combined array-comparative genomic hybridization and single-nucleotide polymorphism-loss of heterozygosity analysis reveals complex genetic alterations in cervical cancer

    Combined array-comparative genomic hybridization and single-nucleotide polymorphism-loss of heterozygosity analysis reveals complex genetic alterations in cervical cancer gan Judith N. Kloth, Jan Oosting, Tom van Wezel, Károly Szuhai, Jeroen Knijnenburg, Arko Gorter, Gemma G. Kenter, Gert Jan Fleuren, Ekaterina S. Jordanova

    Cyhoeddwyd 2007
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  2. 2
    A homozygous deletion of a normal variation locus in a patient with hearing loss from non-consanguineous parents

    A homozygous deletion of a normal variation locus in a patient with hearing loss from non-consanguineous parents gan Jeroen Knijnenburg, Saskia A.J. Lesnik Oberstein, Klemens Frei, Trevor Lucas, A.C.J. Gijsbers, Claudia Ruivenkamp, Hans J. Tanke, Károly Szuhai

    Cyhoeddwyd 2009
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  3. 3
    Diagnosis of genetic abnormalities in developmentally delayed patients: A new strategy combining MLPA and array‐CGH

    Diagnosis of genetic abnormalities in developmentally delayed patients: A new strategy combining MLPA and array‐CGH gan Marjolein Kriek, Jeroen Knijnenburg, Stefan J. White, Carla Rosenberg, Johan T. den Dunnen, Gert‐Jan B. van Ommen, Hans J. Tanke, Martijn H. Breuning, Károly Szuhai

    Cyhoeddwyd 2007
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  4. 4
    Two distinct regions in 2q24.2‐q24.3 associated with idiopathic epilepsy

    Two distinct regions in 2q24.2‐q24.3 associated with idiopathic epilepsy gan Ana Cristina Victorino Krepischi, Jeroen Knijnenburg, Débora Romeo Bertola, Chong Ae Kim, P. Pearson, Emilia Bijlsma, Károly Szuhai, Fernando Kok, Angela Maria Vianna‐Morgante, Carla Rosenberg

    Cyhoeddwyd 2010
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  5. 5
    Oncogenomic analysis of mycosis fungoides reveals major differences with Sézary syndrome

    Oncogenomic analysis of mycosis fungoides reveals major differences with Sézary syndrome gan Remco van Doorn, Marloes S. van Kester, Remco Dijkman, Maarten H. Vermeer, Aat A. Mulder, Károly Szuhai, Jeroen Knijnenburg, Judith M. Boer, Rein Willemze, Cornelis P. Tensen

    Cyhoeddwyd 2008
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  6. 6
    An Xq22.3 duplication detected by comparative genomic hybridization microarray (<i>Array‐CGH</i>) defines a new locus (<i>FGS5</i>) for FG syndrome

    An Xq22.3 duplication detected by comparative genomic hybridization microarray (<i>Array‐CGH</i>) defines a new locus (<i>FGS5</i>) for FG syndrome gan Fernanda Sarquis Jehee, Carla Rosenberg, Ana Cristina Victorino Krepischi, Fernando Kok, Jeroen Knijnenburg, Guy Froyen, Angela Maria Vianna‐Morgante, John M. Opitz, Maria Rita Passos‐Bueno

    Cyhoeddwyd 2005
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  7. 7
    Ring chromosome formation as a novel escape mechanism in patients with inverted duplication and terminal deletion

    Ring chromosome formation as a novel escape mechanism in patients with inverted duplication and terminal deletion gan Jeroen Knijnenburg, Arie van Haeringen, Kerstin Hansson, Arjan C. Lankester, Margot J. M. Smit, René D.M. Belfroid, Egbert Bakker, Carla Rosenberg, Hans J. Tanke, Károly Szuhai

    Cyhoeddwyd 2007
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  8. 8
    Array-Based Comparative Genomic Hybridization Analysis Reveals Recurrent Chromosomal Alterations and Prognostic Parameters in Primary Cutaneous Large B-Cell Lymphoma

    Array-Based Comparative Genomic Hybridization Analysis Reveals Recurrent Chromosomal Alterations and Prognostic Parameters in Primary Cutaneous Large B-Cell Lymphoma gan Remco Dijkman, Cornelis P. Tensen, Ekaterina S. Jordanova, Jeroen Knijnenburg, Juliette J. Hoefnagel, Aat A. Mulder, Carla Rosenberg, Anton K. Raap, Rein Willemze, Károly Szuhai, Maarten H. Vermeer

    Cyhoeddwyd 2005
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  9. 9
    The Role of EXT1 in Nonhereditary Osteochondroma: Identification of Homozygous Deletions

    The Role of EXT1 in Nonhereditary Osteochondroma: Identification of Homozygous Deletions gan Liesbeth Hameetman, Károly Szuhai, Arzu Yavaş, Jeroen Knijnenburg, Mark van Duin, Herman van Dekken, A. H. M. Taminiau, A.M. Cleton-Jansen, Judith V.M.G. Bovée, Pancras C.W. Hogendoorn

    Cyhoeddwyd 2007
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  10. 10
    Chromosome abnormalities in two patients with features of autosomal dominant Robinow syndrome

    Chromosome abnormalities in two patients with features of autosomal dominant Robinow syndrome gan Juliana F. Mazzeu, Ana Cristina Victorino Krepischi, Carla Rosenberg, Károly Szuhai, Jeroen Knijnenburg, Janneke M.M. Weiss, Irina Kerkis, Zan Mustacchi, Guilherme Colin, Rômulo Mombach, Rita de Cássia M. Pavanello, Paulo Alberto Otto, Angela Maria Vianna‐Morgante

    Cyhoeddwyd 2007
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  11. 11
    Chromosome imbalances in syndromic hearing loss

    Chromosome imbalances in syndromic hearing loss gan ALPM Catelani, Ana Cristina Victorino Krepischi, Chong Ae Kim, Fernando Kok, Paulo Alberto Otto, M. T. B. M. Auricchio, Juliana F. Mazzeu, Daniela Tiaki Uehara, SS Costa, Jeroen Knijnenburg, Alfredo Tabith, AM Vianna‐Morgante, RC Mingroni‐Netto, Carla Rosenberg

    Cyhoeddwyd 2009
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  12. 12
    Prenatal SNP array testing in 1000 fetuses with ultrasound anomalies: causative, unexpected and susceptibility CNVs

    Prenatal SNP array testing in 1000 fetuses with ultrasound anomalies: causative, unexpected and susceptibility CNVs gan Malgorzata I. Srebniak, Karin E. M. Diderich, Marieke Joosten, Lutgarde Govaerts, Jeroen Knijnenburg, Femke At de Vries, Marjan Boter, Debora Lont, Maarten F. C. M. Knapen, M. C. de Wit, Attie T. J. I. Go, Robert‐Jan H. Galjaard, Diane Van Opstal

    Cyhoeddwyd 2015
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  13. 13
    Cellular/intramuscular myxoma and grade I myxofibrosarcoma are characterized by distinct genetic alterations and specific composition of their extracellular matrix

    Cellular/intramuscular myxoma and grade I myxofibrosarcoma are characterized by distinct genetic alterations and specific composition of their extracellular matrix gan Stefan M. Willems, Alexander B. Mohseny, Crina I.A. Balog, Raj Sewrajsing, Inge H. Briaire‐de Bruijn, Jeroen Knijnenburg, Anne‐Marie Cleton‐Jansen, Raf Sciot, Christopher D.�M. Fletcher, André M. Deelder, Károly Szuhai, Paul J. Hensbergen, Pancras C.W. Hogendoorn

    Cyhoeddwyd 2009
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  14. 14
    Array-CGH detection of micro rearrangements in mentally retarded individuals: clinical significance of imbalances present both in affected children and normal parents

    Array-CGH detection of micro rearrangements in mentally retarded individuals: clinical significance of imbalances present both in affected children and normal parents gan Carla Rosenberg, Jeroen Knijnenburg, Egbert Bakker, Angela Maria Vianna‐Morgante, Willem C.R. Sloos, Paulo Alberto Otto, Marjolein Kriek, Kerstin Hansson, Ana Cristina Victorino Krepischi, Heike Fiegler, Nigel P. Carter, Emilia K. Bijlsma, Arie van Haeringen, Károly Szuhai, Hans J. Tanke

    Cyhoeddwyd 2005
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  15. 15
    Novel and Highly Recurrent Chromosomal Alterations in Sézary Syndrome

    Novel and Highly Recurrent Chromosomal Alterations in Sézary Syndrome gan Maarten H. Vermeer, Remco van Doorn, Remco Dijkman, Xin Mao, Sean Whittaker, Pieter C. van Voorst Vader, Marie‐Jeanne P. Gerritsen, Marie‐Louise Geerts, Sylke Gellrich, Ola Söderberg, Karl‐Johan Leuchowius, Ulf Landegren, Jacoba J. Out‐Luiting, Jeroen Knijnenburg, Marije IJszenga, Károly Szuhai, Rein Willemze, Cornelis P. Tensen

    Cyhoeddwyd 2008
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  16. 16
    Comprehensive diagnostics of acute myeloid leukemia by whole transcriptome RNA sequencing

    Comprehensive diagnostics of acute myeloid leukemia by whole transcriptome RNA sequencing gan Wibowo Arindrarto, Daniel Borràs, Ruben A. L. de Groen, Redmar R. van den Berg, Irene J. Locher, Saskia A.M.E. van Diessen, Rosalie van der Holst, Edith D. van der Meijden, M. Willy Honders, Rick H. de Leeuw, Wina Verlaat, Inge Jedema, Wilma G. M. Kroes, Jeroen Knijnenburg, Tom van Wezel, Joost S.P. Vermaat, Peter J.M. Valk, Bart Janssen, Peter de Knijff, Cornelis A.M. van Bergen, Erik B. van den Akker, Peter A.C. ‘t Hoen, Szymon M. Kiełbasa, Jeroen F. J. Laros, Marieke Griffioen, Hendrik Veelken

    Cyhoeddwyd 2020
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