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The British Journal of Dermatology
|
October 27, 2010
Dermatological manifestations of inherited cancer syndromes in children
A Karalis, M Tischkowitz, G W M Millington
Clinical Genetics
|
October 14, 2014
Fanconi anaemia: genetics, molecular biology, and cancer – implications for clinical management in children and adults
M Schneider, K Chandler, M Tischkowitz, et al.
Clinical and Experimental Dermatology
|
March 30, 2010
Dermatological features of inherited cancer syndromes in adults
A Al Fares, G W M Millington, M Tischkowitz
Familial Cancer
|
December 15, 2010
Mutation analysis of the PALB2 cancer predisposition gene in familial melanoma
N Sabbaghian, R Kyle, A Hao, et al.
Clinical and Experimental Dermatology
|
January 16, 2018
Evaluation of universal immunohistochemical screening of sebaceous neoplasms in a service setting
K Schon, E Rytina, J Drummond, et al.
Clinical Genetics
|
November 4, 2004
Autosomal dominant B-cell immunodeficiency, distal limb anomalies and urogenital malformations (BILU syndrome) - report of a second family
M Tischkowitz, F Goodman, M Koliou, et al.
Journal of Community Genetics
|
July 6, 2026
Experiences of implementation of personalised risk estimates for breast cancer in clinical practice: a systematic review and qualitative synthesis
N B Fennell, S Abukar, I Kuhn, et al.
Hereditary Cancer in Clinical Practice
|
September 6, 2022
Low-level constitutional mosaicism of BRCA1 in two women with young onset ovarian cancer
B Speight, E Colvin, E D Epurescu, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology
|
June 10, 2000
A comparison of methods currently used in clinical practice to estimate familial breast cancer risks
M Tischkowitz, D Wheeler, E France, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology
|
January 24, 2009
A comparison of models used to predict MLH1, MSH2 and MSH6 mutation carriers
C J Pouchet, N Wong, G Chong, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 23) with videos related to
Sort By:
Page
of 3
The British Journal of Dermatology
|
October 27, 2010
Dermatological manifestations of inherited cancer syndromes in children
A Karalis, M Tischkowitz, G W M Millington
Clinical Genetics
|
October 14, 2014
Fanconi anaemia: genetics, molecular biology, and cancer – implications for clinical management in children and adults
M Schneider, K Chandler, M Tischkowitz, et al.
Clinical and Experimental Dermatology
|
March 30, 2010
Dermatological features of inherited cancer syndromes in adults
A Al Fares, G W M Millington, M Tischkowitz
Familial Cancer
|
December 15, 2010
Mutation analysis of the PALB2 cancer predisposition gene in familial melanoma
N Sabbaghian, R Kyle, A Hao, et al.
Clinical and Experimental Dermatology
|
January 16, 2018
Evaluation of universal immunohistochemical screening of sebaceous neoplasms in a service setting
K Schon, E Rytina, J Drummond, et al.
Clinical Genetics
|
November 4, 2004
Autosomal dominant B-cell immunodeficiency, distal limb anomalies and urogenital malformations (BILU syndrome) - report of a second family
M Tischkowitz, F Goodman, M Koliou, et al.
Journal of Community Genetics
|
July 6, 2026
Experiences of implementation of personalised risk estimates for breast cancer in clinical practice: a systematic review and qualitative synthesis
N B Fennell, S Abukar, I Kuhn, et al.
Hereditary Cancer in Clinical Practice
|
September 6, 2022
Low-level constitutional mosaicism of BRCA1 in two women with young onset ovarian cancer
B Speight, E Colvin, E D Epurescu, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology
|
June 10, 2000
A comparison of methods currently used in clinical practice to estimate familial breast cancer risks
M Tischkowitz, D Wheeler, E France, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology
|
January 24, 2009
A comparison of models used to predict MLH1, MSH2 and MSH6 mutation carriers
C J Pouchet, N Wong, G Chong, et al.
Page
of 3