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Jaran Apold

Showing results (11-20 of 18) with videos related to

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Disease Markers|March 1, 2005
Complete mutation screening and haplotype characterization of the BRCA1 gene in 61 familial breast cancer patients from NorwayPetter Frost, Astanand Jugessur, Jaran Apold, et al.
BMC Medical Genetics|March 3, 2006
The frequent BRCA1 mutation 1135insA has multiple origins: a haplotype study in different populationsTeresa M Rudkin, Nancy Hamel, Maria Galvez, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|July 22, 2005
Immunohistochemistry identifies carriers of mismatch repair gene defects causing hereditary nonpolyposis colorectal cancerAstrid T Stormorken, Inger Marie Bowitz-Lothe, Tove Norèn, et al.
Breast (Edinburgh, Scotland)|February 24, 2007
Sensitivity of MRI versus conventional screening in the diagnosis of BRCA-associated breast cancer in a national prospective seriesAnne I Hagen, Kjell Arne Kvistad, Lovise Maehle, et al.
International Journal of Cancer|May 2, 2007
Surveillance for familial breast cancer: Differences in outcome according to BRCA mutation statusPal Moller, D Gareth Evans, Marta M Reis, et al.
International Journal of Cancer|September 19, 2002
Survival in prospectively ascertained familial breast cancer: analysis of a series stratified by tumour characteristics, BRCA mutations and oophorectomyPål Møller, Ake Borg, D Gareth Evans, et al.
The New England Journal of Medicine|March 23, 2012
Familial diarrhea syndrome caused by an activating GUCY2C mutationTorunn Fiskerstrand, Najla Arshad, Bjørn Ivar Haukanes, et al.
Journal of Medical Genetics|July 29, 2009
Survival in women with MMR mutations and ovarian cancer: a multicentre study in Lynch syndrome kindredsEli Marie Grindedal, Laura Renkonen-Sinisalo, Hans Vasen, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
Disease Markers|March 1, 2005
Complete mutation screening and haplotype characterization of the BRCA1 gene in 61 familial breast cancer patients from NorwayPetter Frost, Astanand Jugessur, Jaran Apold, et al.
BMC Medical Genetics|March 3, 2006
The frequent BRCA1 mutation 1135insA has multiple origins: a haplotype study in different populationsTeresa M Rudkin, Nancy Hamel, Maria Galvez, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|July 22, 2005
Immunohistochemistry identifies carriers of mismatch repair gene defects causing hereditary nonpolyposis colorectal cancerAstrid T Stormorken, Inger Marie Bowitz-Lothe, Tove Norèn, et al.
Breast (Edinburgh, Scotland)|February 24, 2007
Sensitivity of MRI versus conventional screening in the diagnosis of BRCA-associated breast cancer in a national prospective seriesAnne I Hagen, Kjell Arne Kvistad, Lovise Maehle, et al.
International Journal of Cancer|May 2, 2007
Surveillance for familial breast cancer: Differences in outcome according to BRCA mutation statusPal Moller, D Gareth Evans, Marta M Reis, et al.
International Journal of Cancer|September 19, 2002
Survival in prospectively ascertained familial breast cancer: analysis of a series stratified by tumour characteristics, BRCA mutations and oophorectomyPål Møller, Ake Borg, D Gareth Evans, et al.
The New England Journal of Medicine|March 23, 2012
Familial diarrhea syndrome caused by an activating GUCY2C mutationTorunn Fiskerstrand, Najla Arshad, Bjørn Ivar Haukanes, et al.
Journal of Medical Genetics|July 29, 2009
Survival in women with MMR mutations and ovarian cancer: a multicentre study in Lynch syndrome kindredsEli Marie Grindedal, Laura Renkonen-Sinisalo, Hans Vasen, et al.
Pageof 2