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 (21-30 of 81) with videos related to

Pageof 9
Sort By:
Nederlands Tijdschrift Voor Geneeskunde|April 25, 2000
[Patient with Peutz-Jeghers syndrome and liver metastases from an unknown primary tumor]G van der Werf, F H Menko, J J Gille, et al.
American Journal of Obstetrics and Gynecology|February 18, 1998
Clinical and genetic evaluation of thirty ovarian cancer familiesR P Zweemer, R H Verheijen, J J Gille, et al.
Nederlands Tijdschrift Voor Geneeskunde|March 1, 2007
[DNA-based diagnosis of hereditary tumour predisposition]F H Menko, M J L Ligtenberg, T Brouwer, et al.
Nederlands Tijdschrift Voor Geneeskunde|March 4, 1995
[Cloning of the first gene for breast/ovarian cancer (BRCA1), mapping of a second gene locus (BRCA2) and consequences for clinical practice]J C Oosterwijk, P Devilee, E J Meijers-Heijboer, et al.
Nederlands Tijdschrift Voor Geneeskunde|January 10, 2003
[Recommendations for the management of women with an increased genetic risk of gynaecological cancer]R H M Verheijen, H Boonstra, F H Menko, et al.
Leukemia|April 9, 2013
Highly variable clinical manifestations in a large family with a novel GATA2 mutationP G N J Mutsaers, A A van de Loosdrecht, K Tawana, et al.
Gut|April 6, 2007
Is surveillance of the small bowel indicated for Lynch syndrome families?G L ten Kate, J H Kleibeuker, F M Nagengast, et al.
The Quarterly Journal of Medicine|January 1, 1983
Familial benign hypercalcaemia. Study of a large familyF H Menko, O L Bijvoet, J L Fronen, et al.
European Journal of Pediatrics|July 1, 1994
Familial mitochondrial encephalopathy with fetal ultrasonographic ventriculomegaly and intracerebral calcificationsJ F Samson, P G Barth, J I de Vries, et al.
Human Genetics|March 1, 1996
A (G-to-A) mutation in the initiation codon of the proteolipid protein gene causing a relatively mild form of Pelizaeus-Merzbacher disease in a Dutch familyE A Sistermans, I J de Wijs, R F de Coo, et al.
Pageof 9

Showing results (21-30 of 81) with videos related to

Sort By:
Pageof 9
Nederlands Tijdschrift Voor Geneeskunde|April 25, 2000
[Patient with Peutz-Jeghers syndrome and liver metastases from an unknown primary tumor]G van der Werf, F H Menko, J J Gille, et al.
American Journal of Obstetrics and Gynecology|February 18, 1998
Clinical and genetic evaluation of thirty ovarian cancer familiesR P Zweemer, R H Verheijen, J J Gille, et al.
Nederlands Tijdschrift Voor Geneeskunde|March 1, 2007
[DNA-based diagnosis of hereditary tumour predisposition]F H Menko, M J L Ligtenberg, T Brouwer, et al.
Nederlands Tijdschrift Voor Geneeskunde|March 4, 1995
[Cloning of the first gene for breast/ovarian cancer (BRCA1), mapping of a second gene locus (BRCA2) and consequences for clinical practice]J C Oosterwijk, P Devilee, E J Meijers-Heijboer, et al.
Nederlands Tijdschrift Voor Geneeskunde|January 10, 2003
[Recommendations for the management of women with an increased genetic risk of gynaecological cancer]R H M Verheijen, H Boonstra, F H Menko, et al.
Leukemia|April 9, 2013
Highly variable clinical manifestations in a large family with a novel GATA2 mutationP G N J Mutsaers, A A van de Loosdrecht, K Tawana, et al.
Gut|April 6, 2007
Is surveillance of the small bowel indicated for Lynch syndrome families?G L ten Kate, J H Kleibeuker, F M Nagengast, et al.
The Quarterly Journal of Medicine|January 1, 1983
Familial benign hypercalcaemia. Study of a large familyF H Menko, O L Bijvoet, J L Fronen, et al.
European Journal of Pediatrics|July 1, 1994
Familial mitochondrial encephalopathy with fetal ultrasonographic ventriculomegaly and intracerebral calcificationsJ F Samson, P G Barth, J I de Vries, et al.
Human Genetics|March 1, 1996
A (G-to-A) mutation in the initiation codon of the proteolipid protein gene causing a relatively mild form of Pelizaeus-Merzbacher disease in a Dutch familyE A Sistermans, I J de Wijs, R F de Coo, et al.
Pageof 9