Resultats de la cerca - Annelies de Klein

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  1. 1
    Genetics of Uveal Melanoma and Cutaneous Melanoma: Two of a Kind?

    Genetics of Uveal Melanoma and Cutaneous Melanoma: Two of a Kind? per Thomas van den Bosch, Emine Kılıç, Dion Paridaens, Annelies de Klein

    Publicat 2010
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  2. 2
    Etiology of Esophageal Atresia and Tracheoesophageal Fistula: “Mind the Gap”

    Etiology of Esophageal Atresia and Tracheoesophageal Fistula: “Mind the Gap” per Elisabeth M. de Jong, Janine F. Felix, Annelies de Klein, Dick Tibboel

    Publicat 2010
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  3. 3
    Uveal melanoma: Towards a molecular understanding

    Uveal melanoma: Towards a molecular understanding per Kyra N. Smit, Martine J. Jager, Annelies de Klein, Emine Kiliҫ

    Publicat 2019
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  4. 4
    Oncogenic GNAQ mutations are not correlated with disease-free survival in uveal melanoma

    Oncogenic GNAQ mutations are not correlated with disease-free survival in uveal melanoma per Jürgen Bauer, Emine Kılıç, Jolanda Vaarwater, Boris C. Bastian, Claus Garbe, Annelies de Klein

    Publicat 2009
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  5. 5
    Localization of the human c-sis oncogene in Ph1-positive and Ph1- negative chronic myelocytic leukemia by in situ hybridization

    Localization of the human c-sis oncogene in Ph1-positive and Ph1- negative chronic myelocytic leukemia by in situ hybridization per CR Bartram, Annelies de Klein, A Hagemeijer, Gerard C. Grosveld, Nora Heisterkamp, John Groffen

    Publicat 1984
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  6. 6
    Genetic Factors in Congenital Diaphragmatic Hernia

    Genetic Factors in Congenital Diaphragmatic Hernia per Ashley M. Holder, Merel Klaassens, Dick Tibboel, Annelies de Klein, B. Lee, Daryl A. Scott

    Publicat 2007
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  7. 7
    Patient survival in uveal melanoma is not affected by oncogenic mutations in GNAQ and GNA11

    Patient survival in uveal melanoma is not affected by oncogenic mutations in GNAQ and GNA11 per Anna E. Koopmans, Jolanda Vaarwater, Dion Paridaens, Nicole C. Naus, Emine Kılıç, Annelies de Klein

    Publicat 2013
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  8. 8
    Molecular analysis of both translocation products of a Philadelphia-positive CML patient

    Molecular analysis of both translocation products of a Philadelphia-positive CML patient per Annelies de Klein, Ton van Agthoven, Cora Groffen, Nora Heisterkamp, John Groffen, Gerard C. Grosveld

    Publicat 1986
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  9. 9
    C-abl and bcr are rearranged in a Ph1-negative CML patient.

    C-abl and bcr are rearranged in a Ph1-negative CML patient. per Claus R. Bartram, E. Kleihauer, Annelies de Klein, Gerard C. Grosveld, J. Teyssier, Nora Heisterkamp, John Groffen

    Publicat 1985
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  10. 10
    c-sis is translocated from chromosome 22 to chromosome 9 in chronic myelocytic leukemia.

    c-sis is translocated from chromosome 22 to chromosome 9 in chronic myelocytic leukemia. per John Groffen, Nora Heisterkamp, John Stephenson, A G van Kessel, Annelies de Klein, Gerard C. Grosveld, D. Bootsma

    Publicat 1983
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  11. 11
    The chronic myelocytic cell line K562 contains a breakpoint in bcr and produces a chimeric bcr/c-abl transcript.

    The chronic myelocytic cell line K562 contains a breakpoint in bcr and produces a chimeric bcr/c-abl transcript. per Gerard C. Grosveld, T Verwoerd, T van Agthoven, Annelies de Klein, K L Ramachandran, Nora Heisterkamp, Kelly Stam, John Groffen

    Publicat 1986
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  12. 12
    Can we improve outcome of congenital diaphragmatic hernia?

    Can we improve outcome of congenital diaphragmatic hernia? per L. van den Hout, Ilona Sluiter, Saskia J. Gischler, Annelies de Klein, Robbert J. Rottier, Hanneke IJsselstijn, Irwin Reiss, Dick Tibboel

    Publicat 2009
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  13. 13
    Early-onset parkinsonism caused by alpha-synuclein gene triplication: Clinical and genetic findings in a novel family

    Early-onset parkinsonism caused by alpha-synuclein gene triplication: Clinical and genetic findings in a novel family per Simone Olgiati, Astrid Thomas, Marialuisa Quadri, Guido J. Breedveld, Josja Graafland, Hubertus Eussen, Hannie Douben, Annelies de Klein, Marco Onofrj, Vincenzo Bonifati

    Publicat 2015
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  14. 14
    Targeted disruption of the cell-cycle checkpoint gene ATR leads to early embryonic lethality in mice

    Targeted disruption of the cell-cycle checkpoint gene ATR leads to early embryonic lethality in mice per Annelies de Klein, Manja Muijtjens, Ronald van Os, Y. Verhoeven, Bep Smit, Antony M. Carr, Alan R. Lehmann, Jan H.J. Hoeijmakers

    Publicat 2000
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  15. 15
    Clinical geneticists' views of VACTERL/VATER association

    Clinical geneticists' views of VACTERL/VATER association per Benjamin D. Solomon, Kelly Bear, Virginia Kimonis, Annelies de Klein, Daryl A. Scott, Charles Shaw‐Smith, Dick Tibboel, Heiko Reutter, Philip F. Giampietro

    Publicat 2012
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  16. 16
    Genome-wide oligonucleotide-based array comparative genome hybridization analysis of non-isolated congenital diaphragmatic hernia

    Genome-wide oligonucleotide-based array comparative genome hybridization analysis of non-isolated congenital diaphragmatic hernia per Daryl A. Scott, Merel Klaassens, Ashley M. Holder, Kevin P. Lally, Caraciolo J. Fernandes, Robert‐Jan Galjaard, Dick Tibboel, Annelies de Klein, Brendan Lee

    Publicat 2007
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  17. 17
    bcr rearrangement and translocation of the c-abl oncogene in Philadelphia positive acute lymphoblastic leukemia

    bcr rearrangement and translocation of the c-abl oncogene in Philadelphia positive acute lymphoblastic leukemia per Annelies de Klein, A Hagemeijer, CR Bartram, R. H. J. Houwen, L. H. Hoefsloot, Félix Carbonell, Leo Lai Chan, M. Barnett, Mel Greaves, E. Kleihauer

    Publicat 1986
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  18. 18
    Rapid aneuploidy detection with multiplex ligation-dependent probe amplification: a prospective study of 4000 amniotic fluid samples

    Rapid aneuploidy detection with multiplex ligation-dependent probe amplification: a prospective study of 4000 amniotic fluid samples per Diane Van Opstal, Marjan Boter, Daniëlle de Jong, Cardi van den Berg, Hennie T. Brüggenwirth, Hajo I. J. Wildschut, Annelies de Klein, Robert‐Jan H. Galjaard

    Publicat 2008
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  19. 19
    Richter's syndrome with different immunoglobulin light chains and different heavy chain gene rearrangements

    Richter's syndrome with different immunoglobulin light chains and different heavy chain gene rearrangements per JJ van Dongen, Herbert Hooijkaas, Michiels Jj, Gerard C. Grosveld, Annelies de Klein, Theodorus van der Kwast, M. E. F. Prins, J. Abels, A Hagemeijer

    Publicat 1984
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  20. 20
    Alveolar capillary dysplasia with misalignment of the pulmonary veins: clinical, histological, and genetic aspects

    Alveolar capillary dysplasia with misalignment of the pulmonary veins: clinical, histological, and genetic aspects per E Slot, Gabriëla G. Edel, Ernest Cutz, Arno van Heijst, Martin Post, J. Marco Schnater, René Wijnen, Dick Tibboel, Robbert J. Rottier, Annelies de Klein

    Publicat 2018
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