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Clinical and Experimental Immunology
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March 3, 2011
Enhanced lymphocyte interferon (IFN)-γ responses in a PTEN mutation-negative Cowden disease kindred
R Stevenson, A Fatehullah, I Jagan, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
January 22, 2014
Malformation risks of antiepileptic drug monotherapies in pregnancy: updated results from the UK and Ireland Epilepsy and Pregnancy Registers
E Campbell, F Kennedy, A Russell, et al.
Genetic Testing
|
May 14, 2004
Non-uptake of predictive genetic testing for BRCA1/2 among relatives of known carriers: attributes, cancer worry, and barriers to testing in a multicenter clinical cohort
C Foster, D G R Evans, R Eeles, et al.
Disease Markers
|
December 14, 1999
Genetic testing for breast cancer predisposition in 1999: which molecular strategy and which family criteria?
D Stoppa-Lyonnet, M Caligo, D Eccles, et al.
Disease Markers
|
December 14, 1999
Insurance implications for individuals with a high risk of breast and ovarian cancer in Europe
P J Morrison, C M Steel, H F Vasen, et al.
Journal of Medical Genetics
|
April 4, 2006
Exonic STK11 deletions are not a rare cause of Peutz-Jeghers syndrome
N C M Hearle, M F Rudd, W Lim, et al.
Seizure
|
July 17, 2021
Zonisamide safety in pregnancy: Data from the UK and Ireland epilepsy and pregnancy register
G McCluskey, M O Kinney, A Russell, et al.
Journal of Medical Genetics
|
April 17, 2008
Predicting the likelihood of carrying a BRCA1 or BRCA2 mutation: validation of BOADICEA, BRCAPRO, IBIS, Myriad and the Manchester scoring system using data from UK genetics clinics
A C Antoniou, R Hardy, L Walker, et al.
Journal of Medical Genetics
|
March 16, 2007
Reduced penetrance alleles for Huntington's disease: a multi-centre direct observational study
Oliver W J Quarrell, Alan S Rigby, L Barron, et al.
Journal of Medical Genetics
|
November 11, 2008
Risk reducing mastectomy: outcomes in 10 European centres
D G R Evans, A D Baildam, E Anderson, et al.
Page
of 16
Search research articles
Search
Showing results (141-150 of 155) with videos related to
Sort By:
Page
of 16
Clinical and Experimental Immunology
|
March 3, 2011
Enhanced lymphocyte interferon (IFN)-γ responses in a PTEN mutation-negative Cowden disease kindred
R Stevenson, A Fatehullah, I Jagan, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
January 22, 2014
Malformation risks of antiepileptic drug monotherapies in pregnancy: updated results from the UK and Ireland Epilepsy and Pregnancy Registers
E Campbell, F Kennedy, A Russell, et al.
Genetic Testing
|
May 14, 2004
Non-uptake of predictive genetic testing for BRCA1/2 among relatives of known carriers: attributes, cancer worry, and barriers to testing in a multicenter clinical cohort
C Foster, D G R Evans, R Eeles, et al.
Disease Markers
|
December 14, 1999
Genetic testing for breast cancer predisposition in 1999: which molecular strategy and which family criteria?
D Stoppa-Lyonnet, M Caligo, D Eccles, et al.
Disease Markers
|
December 14, 1999
Insurance implications for individuals with a high risk of breast and ovarian cancer in Europe
P J Morrison, C M Steel, H F Vasen, et al.
Journal of Medical Genetics
|
April 4, 2006
Exonic STK11 deletions are not a rare cause of Peutz-Jeghers syndrome
N C M Hearle, M F Rudd, W Lim, et al.
Seizure
|
July 17, 2021
Zonisamide safety in pregnancy: Data from the UK and Ireland epilepsy and pregnancy register
G McCluskey, M O Kinney, A Russell, et al.
Journal of Medical Genetics
|
April 17, 2008
Predicting the likelihood of carrying a BRCA1 or BRCA2 mutation: validation of BOADICEA, BRCAPRO, IBIS, Myriad and the Manchester scoring system using data from UK genetics clinics
A C Antoniou, R Hardy, L Walker, et al.
Journal of Medical Genetics
|
March 16, 2007
Reduced penetrance alleles for Huntington's disease: a multi-centre direct observational study
Oliver W J Quarrell, Alan S Rigby, L Barron, et al.
Journal of Medical Genetics
|
November 11, 2008
Risk reducing mastectomy: outcomes in 10 European centres
D G R Evans, A D Baildam, E Anderson, et al.
Page
of 16