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

Yvonne M C Hendriks

Showing results (1-10 of 16) with videos related to

Pageof 2
Sort By:
Clinical Endocrinology|June 30, 2015
Positive effect of growth hormone treatment in maternal uniparental disomy chromosome 14Susanne E Stalman, Gerdine A Kamp, Yvonne M C Hendriks, et al.
Nederlands Tijdschrift Voor Geneeskunde|April 23, 2015
[Maternal uniparental disomy 14; differential diagnosis with Prader-Willi syndrome]Saskia Tamminga, Susanne E Stalman, Gerdine A Kamp, et al.
Hormone Research in Paediatrics|January 24, 2015
WT1 deletion leading to severe 46,XY gonadal dysgenesis, Wilms tumor and gonadoblastoma: case reportMartijn J J Finken, Yvonne M C Hendriks, J Patrick van der Voorn, et al.
CA: a Cancer Journal for Clinicians|July 28, 2006
Diagnostic approach and management of Lynch syndrome (hereditary nonpolyposis colorectal carcinoma): a guide for cliniciansYvonne M C Hendriks, Andrea E de Jong, Hans Morreau, et al.
Gastroenterology|March 15, 2006
Decrease in mortality in Lynch syndrome families because of surveillanceAndrea E de Jong, Yvonne M C Hendriks, Jan H Kleibeuker, et al.
American Journal of Medical Genetics. Part A|March 16, 2013
GPSM2 and Chudley-McCullough syndrome: a Dutch founder variant brought to North AmericaRowida Almomani, Yu Sun, Emmelien Aten, et al.
Familial Cancer|October 14, 2006
The natural history of a combined defect in MSH6 and MUTYH in a HNPCC familyMarjo van Puijenbroek, Maartje Nielsen, Tjitske H C M Reinards, et al.
The Journal of Clinical Endocrinology and Metabolism|May 27, 2025
Clinical Characteristics and Response to Growth Hormone Treatment in 27 Children With Heterozygous NPR2 Variants: Real-World DataJudith S Renes, Ardine M J Reedijk, Anita C S Hokken-Koelega, et al.
Gastroenterology|February 14, 2006
Heterozygous mutations in PMS2 cause hereditary nonpolyposis colorectal carcinoma (Lynch syndrome)Yvonne M C Hendriks, Shantie Jagmohan-Changur, Heleen M van der Klift, et al.
Hormone Research in Paediatrics|June 5, 2024
Genetic Findings in Short Turkish Children Born to Consanguineous ParentsSjoerd D Joustra, Emregul Isik, Jan M Wit, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Clinical Endocrinology|June 30, 2015
Positive effect of growth hormone treatment in maternal uniparental disomy chromosome 14Susanne E Stalman, Gerdine A Kamp, Yvonne M C Hendriks, et al.
Nederlands Tijdschrift Voor Geneeskunde|April 23, 2015
[Maternal uniparental disomy 14; differential diagnosis with Prader-Willi syndrome]Saskia Tamminga, Susanne E Stalman, Gerdine A Kamp, et al.
Hormone Research in Paediatrics|January 24, 2015
WT1 deletion leading to severe 46,XY gonadal dysgenesis, Wilms tumor and gonadoblastoma: case reportMartijn J J Finken, Yvonne M C Hendriks, J Patrick van der Voorn, et al.
CA: a Cancer Journal for Clinicians|July 28, 2006
Diagnostic approach and management of Lynch syndrome (hereditary nonpolyposis colorectal carcinoma): a guide for cliniciansYvonne M C Hendriks, Andrea E de Jong, Hans Morreau, et al.
Gastroenterology|March 15, 2006
Decrease in mortality in Lynch syndrome families because of surveillanceAndrea E de Jong, Yvonne M C Hendriks, Jan H Kleibeuker, et al.
American Journal of Medical Genetics. Part A|March 16, 2013
GPSM2 and Chudley-McCullough syndrome: a Dutch founder variant brought to North AmericaRowida Almomani, Yu Sun, Emmelien Aten, et al.
Familial Cancer|October 14, 2006
The natural history of a combined defect in MSH6 and MUTYH in a HNPCC familyMarjo van Puijenbroek, Maartje Nielsen, Tjitske H C M Reinards, et al.
The Journal of Clinical Endocrinology and Metabolism|May 27, 2025
Clinical Characteristics and Response to Growth Hormone Treatment in 27 Children With Heterozygous NPR2 Variants: Real-World DataJudith S Renes, Ardine M J Reedijk, Anita C S Hokken-Koelega, et al.
Gastroenterology|February 14, 2006
Heterozygous mutations in PMS2 cause hereditary nonpolyposis colorectal carcinoma (Lynch syndrome)Yvonne M C Hendriks, Shantie Jagmohan-Changur, Heleen M van der Klift, et al.
Hormone Research in Paediatrics|June 5, 2024
Genetic Findings in Short Turkish Children Born to Consanguineous ParentsSjoerd D Joustra, Emregul Isik, Jan M Wit, et al.
Pageof 2