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Familial Cancer
|
July 20, 2007
BRCA1/2 mutation analysis in male breast cancer families from North West England
D G R Evans, Mike Bulman, Karen Young, et al.
Lancet (London, England)
|
April 4, 2003
Prediction of pathogenic mutations in patients with early-onset breast cancer by family history
Fiona Lalloo, Jennifer Varley, David Ellis, et al.
Journal of Medical Genetics
|
February 25, 2012
Life expectancy in hereditary cancer predisposing diseases: an observational study
Anna Wilding, Sarah Louise Ingham, Fiona Lalloo, et al.
Journal of Medical Genetics
|
March 9, 2023
<i>MSH2</i> is the very young onset ovarian cancer predisposition gene, not <i>BRCA1</i>
Nicola Flaum, Emma J Crosbie, Emma Roisin Woodward, et al.
BMC Medical Informatics and Decision Making
|
October 3, 2014
Can multiple SNP testing in BRCA2 and BRCA1 female carriers be used to improve risk prediction models in conjunction with clinical assessment?
Mattia C F Prosperi, Sarah L Ingham, Anthony Howell, et al.
Familial Cancer
|
March 13, 2024
Cascade screening in HBOC and Lynch syndrome: guidelines and procedures in a UK centre
D Gareth Evans, Kate Green, George J Burghel, et al.
European Journal of Human Genetics : EJHG
|
September 25, 2014
A clinical and genetic analysis of multiple primary cancer referrals to genetics services
James Whitworth, Jon Hoffman, Cyril Chapman, et al.
Breast Cancer Research and Treatment
|
June 21, 2013
Contralateral mastectomy improves survival in women with BRCA1/2-associated breast cancer
D Gareth R Evans, Sarah L Ingham, Andrew Baildam, et al.
Journal of Medical Genetics
|
June 24, 2015
Lynch syndrome caused by MLH1 mutations is associated with an increased risk of breast cancer: a cohort study
Elaine F Harkness, Emma Barrow, Katy Newton, et al.
Familial Cancer
|
June 25, 2021
Surveillance recommendations for DICER1 pathogenic variant carriers: a report from the SIOPE Host Genome Working Group and CanGene-CanVar Clinical Guideline Working Group
Jette J Bakhuizen, Helen Hanson, Karin van der Tuin, et al.
Page
of 17
Search research articles
Search
Showing results (21-30 of 162) with videos related to
Sort By:
Page
of 17
Familial Cancer
|
July 20, 2007
BRCA1/2 mutation analysis in male breast cancer families from North West England
D G R Evans, Mike Bulman, Karen Young, et al.
Lancet (London, England)
|
April 4, 2003
Prediction of pathogenic mutations in patients with early-onset breast cancer by family history
Fiona Lalloo, Jennifer Varley, David Ellis, et al.
Journal of Medical Genetics
|
February 25, 2012
Life expectancy in hereditary cancer predisposing diseases: an observational study
Anna Wilding, Sarah Louise Ingham, Fiona Lalloo, et al.
Journal of Medical Genetics
|
March 9, 2023
<i>MSH2</i> is the very young onset ovarian cancer predisposition gene, not <i>BRCA1</i>
Nicola Flaum, Emma J Crosbie, Emma Roisin Woodward, et al.
BMC Medical Informatics and Decision Making
|
October 3, 2014
Can multiple SNP testing in BRCA2 and BRCA1 female carriers be used to improve risk prediction models in conjunction with clinical assessment?
Mattia C F Prosperi, Sarah L Ingham, Anthony Howell, et al.
Familial Cancer
|
March 13, 2024
Cascade screening in HBOC and Lynch syndrome: guidelines and procedures in a UK centre
D Gareth Evans, Kate Green, George J Burghel, et al.
European Journal of Human Genetics : EJHG
|
September 25, 2014
A clinical and genetic analysis of multiple primary cancer referrals to genetics services
James Whitworth, Jon Hoffman, Cyril Chapman, et al.
Breast Cancer Research and Treatment
|
June 21, 2013
Contralateral mastectomy improves survival in women with BRCA1/2-associated breast cancer
D Gareth R Evans, Sarah L Ingham, Andrew Baildam, et al.
Journal of Medical Genetics
|
June 24, 2015
Lynch syndrome caused by MLH1 mutations is associated with an increased risk of breast cancer: a cohort study
Elaine F Harkness, Emma Barrow, Katy Newton, et al.
Familial Cancer
|
June 25, 2021
Surveillance recommendations for DICER1 pathogenic variant carriers: a report from the SIOPE Host Genome Working Group and CanGene-CanVar Clinical Guideline Working Group
Jette J Bakhuizen, Helen Hanson, Karin van der Tuin, et al.
Page
of 17