Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

F H Menko

Showing results (61-70 of 81) with videos related to

Pageof 9
Sort By:
European Journal of Cancer (Oxford, England : 1990)|May 29, 2007
Humoral immune responses to MUC1 in women with a BRCA1 or BRCA2 mutationB B J Hermsen, R H M Verheijen, F H Menko, et al.
Journal of Clinical Pathology|April 11, 2006
Distinction between hereditary and sporadic breast cancer on the basis of clinicopathological dataP van der Groep, A Bouter, R van der Zanden, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|October 13, 2001
Comparative genomic hybridization of microdissected familial ovarian carcinoma: two deleted regions on chromosome 15q not previously identified in sporadic ovarian carcinomaR P Zweemer, A Ryan, A M Snijders, et al.
Journal of Clinical Pathology|September 29, 2005
STRAD in Peutz-Jeghers syndrome and sporadic cancersW W J de Leng, J J Keller, S Luiten, et al.
Gastroenterology|April 1, 1996
Cancer risk in families with hereditary nonpolyposis colorectal cancer diagnosed by mutation analysisH F Vasen, J T Wijnen, F H Menko, et al.
British Journal of Cancer|October 10, 2002
Genomic deletions of MSH2 and MLH1 in colorectal cancer families detected by a novel mutation detection approachJ J P Gille, F B L Hogervorst, G Pals, et al.
Oncogene|November 9, 2010
Absence of the Birt-Hogg-Dubé gene product is associated with increased hypoxia-inducible factor transcriptional activity and a loss of metabolic flexibilityR S Preston, A Philp, T Claessens, et al.
Clinical Genetics|January 26, 2011
Childhood brain tumours due to germline bi-allelic mismatch repair gene mutationsP C Johannesma, H M van der Klift, N C T van Grieken, et al.
Journal of Medical Genetics|July 6, 2004
Constitutional rearrangements of chromosome 22 as a cause of neurofibromatosis 2T Tsilchorozidou, F H Menko, F Lalloo, et al.
Familial Cancer|June 20, 2024
Metastatic disease after removal of a renal cell carcinoma smaller than 3 cm in a patient with Birt-Hogg-Dubé syndrome, a case reportL van Riel, C M Kets, L P van Hest, et al.
Pageof 9

Showing results (61-70 of 81) with videos related to

Sort By:
Pageof 9
European Journal of Cancer (Oxford, England : 1990)|May 29, 2007
Humoral immune responses to MUC1 in women with a BRCA1 or BRCA2 mutationB B J Hermsen, R H M Verheijen, F H Menko, et al.
Journal of Clinical Pathology|April 11, 2006
Distinction between hereditary and sporadic breast cancer on the basis of clinicopathological dataP van der Groep, A Bouter, R van der Zanden, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|October 13, 2001
Comparative genomic hybridization of microdissected familial ovarian carcinoma: two deleted regions on chromosome 15q not previously identified in sporadic ovarian carcinomaR P Zweemer, A Ryan, A M Snijders, et al.
Journal of Clinical Pathology|September 29, 2005
STRAD in Peutz-Jeghers syndrome and sporadic cancersW W J de Leng, J J Keller, S Luiten, et al.
Gastroenterology|April 1, 1996
Cancer risk in families with hereditary nonpolyposis colorectal cancer diagnosed by mutation analysisH F Vasen, J T Wijnen, F H Menko, et al.
British Journal of Cancer|October 10, 2002
Genomic deletions of MSH2 and MLH1 in colorectal cancer families detected by a novel mutation detection approachJ J P Gille, F B L Hogervorst, G Pals, et al.
Oncogene|November 9, 2010
Absence of the Birt-Hogg-Dubé gene product is associated with increased hypoxia-inducible factor transcriptional activity and a loss of metabolic flexibilityR S Preston, A Philp, T Claessens, et al.
Clinical Genetics|January 26, 2011
Childhood brain tumours due to germline bi-allelic mismatch repair gene mutationsP C Johannesma, H M van der Klift, N C T van Grieken, et al.
Journal of Medical Genetics|July 6, 2004
Constitutional rearrangements of chromosome 22 as a cause of neurofibromatosis 2T Tsilchorozidou, F H Menko, F Lalloo, et al.
Familial Cancer|June 20, 2024
Metastatic disease after removal of a renal cell carcinoma smaller than 3 cm in a patient with Birt-Hogg-Dubé syndrome, a case reportL van Riel, C M Kets, L P van Hest, et al.
Pageof 9