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The Journal of Molecular Diagnostics : JMD
|
January 26, 2007
A complex rearrangement in the APC gene uncovered by multiplex ligation-dependent probe amplification
Constanze Pagenstecher, Dorothea Gadzicki, Dietlinde Stienen, et al.
Journal of Community Genetics
|
November 24, 2011
Genetic testing for familial/hereditary breast cancer-comparison of guidelines and recommendations from the UK, France, the Netherlands and Germany
Dorothea Gadzicki, D Gareth Evans, Hilary Harris, et al.
The Journal of Pathology
|
February 5, 2009
Comprehensive genetic and functional characterization of IPH-926: a novel CDH1-null tumour cell line from human lobular breast cancer
Matthias Christgen, Henriette Bruchhardt, Catarina Hadamitzky, et al.
European Journal of Medical Genetics
|
July 14, 2010
Novel CHD7 mutations contributing to the mutation spectrum in patients with CHARGE syndrome
Kathrin Wessels, Bettina Bohnhorst, Ingrid Luhmer, et al.
International Journal of Cancer
|
April 13, 2011
Association of death receptor 4 variant (683A > C) with ovarian cancer risk in BRCA1 mutation carriers
Michelle G Dick, Beatrix Versmold, Christoph Engel, et al.
Breast Cancer Research : BCR
|
December 11, 2012
The risk of contralateral breast cancer in patients from BRCA1/2 negative high risk families as compared to patients from BRCA1 or BRCA2 positive families: a retrospective cohort study
Kerstin Rhiem, Christoph Engel, Monika Graeser, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
October 28, 2009
Contralateral breast cancer risk in BRCA1 and BRCA2 mutation carriers
Monika K Graeser, Christoph Engel, Kerstin Rhiem, et al.
Journal of Medical Genetics
|
April 9, 2013
Evaluating the performance of the breast cancer genetic risk models BOADICEA, IBIS, BRCAPRO and Claus for predicting BRCA1/2 mutation carrier probabilities: a study based on 7352 families from the German Hereditary Breast and Ovarian Cancer Consortium
Christine Fischer, Karoline Kuchenbäcker, Christoph Engel, et al.
International Journal of Cancer
|
October 27, 2009
Low-risk variants FGFR2, TNRC9 and LSP1 in German familial breast cancer patients
Kari Hemminki, Bertram Müller-Myhsok, Peter Lichtner, et al.
American Journal of Medical Genetics. Part A
|
February 5, 2016
Clinical delineation of the PACS1-related syndrome--Report on 19 patients
Janneke H M Schuurs-Hoeijmakers, Megan L Landsverk, Nicola Foulds, et al.
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Search research articles
Search
Showing results (11-20 of 32) with videos related to
Sort By:
Page
of 4
The Journal of Molecular Diagnostics : JMD
|
January 26, 2007
A complex rearrangement in the APC gene uncovered by multiplex ligation-dependent probe amplification
Constanze Pagenstecher, Dorothea Gadzicki, Dietlinde Stienen, et al.
Journal of Community Genetics
|
November 24, 2011
Genetic testing for familial/hereditary breast cancer-comparison of guidelines and recommendations from the UK, France, the Netherlands and Germany
Dorothea Gadzicki, D Gareth Evans, Hilary Harris, et al.
The Journal of Pathology
|
February 5, 2009
Comprehensive genetic and functional characterization of IPH-926: a novel CDH1-null tumour cell line from human lobular breast cancer
Matthias Christgen, Henriette Bruchhardt, Catarina Hadamitzky, et al.
European Journal of Medical Genetics
|
July 14, 2010
Novel CHD7 mutations contributing to the mutation spectrum in patients with CHARGE syndrome
Kathrin Wessels, Bettina Bohnhorst, Ingrid Luhmer, et al.
International Journal of Cancer
|
April 13, 2011
Association of death receptor 4 variant (683A > C) with ovarian cancer risk in BRCA1 mutation carriers
Michelle G Dick, Beatrix Versmold, Christoph Engel, et al.
Breast Cancer Research : BCR
|
December 11, 2012
The risk of contralateral breast cancer in patients from BRCA1/2 negative high risk families as compared to patients from BRCA1 or BRCA2 positive families: a retrospective cohort study
Kerstin Rhiem, Christoph Engel, Monika Graeser, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
October 28, 2009
Contralateral breast cancer risk in BRCA1 and BRCA2 mutation carriers
Monika K Graeser, Christoph Engel, Kerstin Rhiem, et al.
Journal of Medical Genetics
|
April 9, 2013
Evaluating the performance of the breast cancer genetic risk models BOADICEA, IBIS, BRCAPRO and Claus for predicting BRCA1/2 mutation carrier probabilities: a study based on 7352 families from the German Hereditary Breast and Ovarian Cancer Consortium
Christine Fischer, Karoline Kuchenbäcker, Christoph Engel, et al.
International Journal of Cancer
|
October 27, 2009
Low-risk variants FGFR2, TNRC9 and LSP1 in German familial breast cancer patients
Kari Hemminki, Bertram Müller-Myhsok, Peter Lichtner, et al.
American Journal of Medical Genetics. Part A
|
February 5, 2016
Clinical delineation of the PACS1-related syndrome--Report on 19 patients
Janneke H M Schuurs-Hoeijmakers, Megan L Landsverk, Nicola Foulds, et al.
Page
of 4