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Dorothea Gadzicki

Showing results (1-10 of 32) with videos related to

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Leukemia Research|December 22, 2009
Recurrent involvement of heterochromatic regions in multiple myeloma-a multicolor FISH studyKathrin Lange, Dorothea Gadzicki, Brigitte Schlegelberger, et al.
European Journal of Human Genetics : EJHG|March 8, 2007
Diagnostic accuracy of methods for the detection of BRCA1 and BRCA2 mutations: a systematic reviewAnsgar Gerhardus, Henriette Schleberger, Brigitte Schlegelberger, et al.
European Journal of Human Genetics : EJHG|December 19, 2008
Breast cancer susceptibility: current knowledge and implications for genetic counsellingTim Ripperger, Dorothea Gadzicki, Alfons Meindl, et al.
Familial Cancer|August 7, 2012
No evidence for breast cancer susceptibility associated with variants of BRD7, a component of p53 and BRCA1 pathwaysJudith Penkert, Brigitte Schlegelberger, Doris Steinemann, et al.
Virchows Archiv : an International Journal of Pathology|June 11, 2005
Standardised fluorescence in situ hybridisation in cytological and histological specimensLudwig Wilkens, Heidrun Gerr, Dorothea Gadzicki, et al.
Pathobiology : Journal of Immunopathology, Molecular and Cellular Biology|March 22, 2007
Fluorescence in situ hybridization reveals closely correlated results in cytological and histological specimens of hematological neoplasias compared to conventional cytogeneticsHeidrun Gerr, Dorothea Gadzicki, Hans Kreipe, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 27, 2004
Tourette syndrome is not caused by mutations in the central cannabinoid receptor (CNR1) geneDorothea Gadzicki, Kirsten R Müller-Vahl, Daniela Heller, et al.
European Journal of Medical Genetics|July 11, 2006
Hereditary hemorrhagic telangiectasia is caused by the Q490X mutation of the ACVRL1 gene in a large Arab family: support of homozygous lethalityEl-Harith A El-Harith, Wolfgang Kühnau, Jörg Schmidtke, et al.
Cancer Genetics and Cytogenetics|May 19, 2005
BCR-ABL gene amplification and overexpression in a patient with chronic myeloid leukemia treated with imatinibDorothea Gadzicki, Nils von Neuhoff, Doris Steinemann, et al.
Cancer Genetics and Cytogenetics|February 14, 2009
Histopathological criteria and selection algorithms for BRCA1 genetic testingDorothea Gadzicki, Alexandra Schubert, Christine Fischer, et al.
Pageof 4

Showing results (1-10 of 32) with videos related to

Sort By:
Pageof 4
Leukemia Research|December 22, 2009
Recurrent involvement of heterochromatic regions in multiple myeloma-a multicolor FISH studyKathrin Lange, Dorothea Gadzicki, Brigitte Schlegelberger, et al.
European Journal of Human Genetics : EJHG|March 8, 2007
Diagnostic accuracy of methods for the detection of BRCA1 and BRCA2 mutations: a systematic reviewAnsgar Gerhardus, Henriette Schleberger, Brigitte Schlegelberger, et al.
European Journal of Human Genetics : EJHG|December 19, 2008
Breast cancer susceptibility: current knowledge and implications for genetic counsellingTim Ripperger, Dorothea Gadzicki, Alfons Meindl, et al.
Familial Cancer|August 7, 2012
No evidence for breast cancer susceptibility associated with variants of BRD7, a component of p53 and BRCA1 pathwaysJudith Penkert, Brigitte Schlegelberger, Doris Steinemann, et al.
Virchows Archiv : an International Journal of Pathology|June 11, 2005
Standardised fluorescence in situ hybridisation in cytological and histological specimensLudwig Wilkens, Heidrun Gerr, Dorothea Gadzicki, et al.
Pathobiology : Journal of Immunopathology, Molecular and Cellular Biology|March 22, 2007
Fluorescence in situ hybridization reveals closely correlated results in cytological and histological specimens of hematological neoplasias compared to conventional cytogeneticsHeidrun Gerr, Dorothea Gadzicki, Hans Kreipe, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 27, 2004
Tourette syndrome is not caused by mutations in the central cannabinoid receptor (CNR1) geneDorothea Gadzicki, Kirsten R Müller-Vahl, Daniela Heller, et al.
European Journal of Medical Genetics|July 11, 2006
Hereditary hemorrhagic telangiectasia is caused by the Q490X mutation of the ACVRL1 gene in a large Arab family: support of homozygous lethalityEl-Harith A El-Harith, Wolfgang Kühnau, Jörg Schmidtke, et al.
Cancer Genetics and Cytogenetics|May 19, 2005
BCR-ABL gene amplification and overexpression in a patient with chronic myeloid leukemia treated with imatinibDorothea Gadzicki, Nils von Neuhoff, Doris Steinemann, et al.
Cancer Genetics and Cytogenetics|February 14, 2009
Histopathological criteria and selection algorithms for BRCA1 genetic testingDorothea Gadzicki, Alexandra Schubert, Christine Fischer, et al.
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