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Pediatric Blood & Cancer
|
December 14, 2004
Nijmegen breakage syndrome diagnosed as Fanconi anaemia
Helen V New, C M Cale, M Tischkowitz, et al.
Journal of Genetic Counseling
|
July 5, 2015
Genetic Testing Considerations in Breast Cancer Patients
L France, J Gray, G Elwyn, et al.
Oncogenesis
|
February 12, 2014
Serum levels of mature microRNAs in DICER1-mutated pleuropulmonary blastoma
M J Murray, S Bailey, K L Raby, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology
|
July 10, 2024
Population-based germline breast cancer gene association studies and meta-analysis to inform wider mainstream testing
C F Rowlands, S Allen, J Balmaña, et al.
Seminars in Oncology
|
September 29, 2018
Rapid disease progression in a patient with mismatch repair-deficient and cortisol secreting adrenocortical carcinoma treated with pembrolizumab
R T Casey, O Giger, I Seetho, et al.
Clinical Genetics
|
December 16, 2010
Characterization of two Ashkenazi Jewish founder mutations in MSH6 gene causing Lynch syndrome
L Raskin, F Schwenter, M Freytsis, et al.
Oncogene
|
March 21, 2017
Compromised BRCA1-PALB2 interaction is associated with breast cancer risk
T K Foo, M Tischkowitz, S Simhadri, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
July 7, 2021
Clinical likelihood ratios and balanced accuracy for 44 in silico tools against multiple large-scale functional assays of cancer susceptibility genes
C Cubuk, A Garrett, S Choi, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology
|
June 16, 2025
Breast cancer germline multigene panel testing in mainstream oncology based on clinical-public health utility: ESMO Precision Oncology Working Group recommendations
C Turnbull, M I Achatz, J Balmaña, et al.
Journal of the National Cancer Institute
|
August 17, 2000
Randomized trial of a specialist genetic assessment service for familial breast cancer
K Brain, J Gray, P Norman, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 23) with videos related to
Sort By:
Page
of 3
Pediatric Blood & Cancer
|
December 14, 2004
Nijmegen breakage syndrome diagnosed as Fanconi anaemia
Helen V New, C M Cale, M Tischkowitz, et al.
Journal of Genetic Counseling
|
July 5, 2015
Genetic Testing Considerations in Breast Cancer Patients
L France, J Gray, G Elwyn, et al.
Oncogenesis
|
February 12, 2014
Serum levels of mature microRNAs in DICER1-mutated pleuropulmonary blastoma
M J Murray, S Bailey, K L Raby, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology
|
July 10, 2024
Population-based germline breast cancer gene association studies and meta-analysis to inform wider mainstream testing
C F Rowlands, S Allen, J Balmaña, et al.
Seminars in Oncology
|
September 29, 2018
Rapid disease progression in a patient with mismatch repair-deficient and cortisol secreting adrenocortical carcinoma treated with pembrolizumab
R T Casey, O Giger, I Seetho, et al.
Clinical Genetics
|
December 16, 2010
Characterization of two Ashkenazi Jewish founder mutations in MSH6 gene causing Lynch syndrome
L Raskin, F Schwenter, M Freytsis, et al.
Oncogene
|
March 21, 2017
Compromised BRCA1-PALB2 interaction is associated with breast cancer risk
T K Foo, M Tischkowitz, S Simhadri, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
July 7, 2021
Clinical likelihood ratios and balanced accuracy for 44 in silico tools against multiple large-scale functional assays of cancer susceptibility genes
C Cubuk, A Garrett, S Choi, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology
|
June 16, 2025
Breast cancer germline multigene panel testing in mainstream oncology based on clinical-public health utility: ESMO Precision Oncology Working Group recommendations
C Turnbull, M I Achatz, J Balmaña, et al.
Journal of the National Cancer Institute
|
August 17, 2000
Randomized trial of a specialist genetic assessment service for familial breast cancer
K Brain, J Gray, P Norman, et al.
Page
of 3