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

M Maas

Showing results (691-700 of 743) with videos related to

Pageof 75
Sort By:
Clinical Epigenetics|November 6, 2019
A genome-wide DNA methylation signature for SETD1B-related syndromeI M Krzyzewska, S M Maas, P Henneman, et al.
Hypertension (Dallas, Tex. : 1979)|July 9, 2020
Pregnancy-Related Complications in Patients With Fibromuscular Dysplasia: A Report From the European/International Fibromuscular Dysplasia RegistryMarco Pappaccogli, Aleksander Prejbisz, Simina Ciurică, et al.
BMC Cancer|August 20, 2015
Early salpingectomy (TUbectomy) with delayed oophorectomy to improve quality of life as alternative for risk-reducing salpingo-oophorectomy in BRCA1/2 mutation carriers (TUBA study): a prospective non-randomised multicentre studyMarline G Harmsen, Marieke Arts-de Jong, Nicoline Hoogerbrugge, et al.
Human Genetics|December 12, 2013
X-linked congenital ptosis and associated intellectual disability, short stature, microcephaly, cleft palate, digital and genital abnormalities define novel Xq25q26 duplication syndromeR S Møller, L R Jensen, S M Maas, et al.
American Journal of Human Genetics|November 24, 2020
Heterozygous Variants in KDM4B Lead to Global Developmental Delay and Neuroanatomical DefectsAnna R Duncan, Antonio Vitobello, Stephan C Collins, et al.
European Journal of Human Genetics : EJHG|March 31, 2025
DDX3X-related neurodevelopmental disorder in males - presenting a new cohort of 19 males and a literature reviewMilou G P Kennis, Dmitrijs Rots, Arjan Bouman, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 8, 2026
Clinical, Genetic, and Imaging Characteristics of SCA27B: Insights from a Large Dutch CohortTeije H van Prooije, Maartje Pennings, Roderick P P W M Maas, et al.
Clinical Epigenetics|August 1, 2024
Multi-locus imprinting disturbance (MLID): interim joint statement for clinical and molecular diagnosisDeborah J G Mackay, Gabriella Gazdagh, David Monk, et al.
Human Reproduction (Oxford, England)|August 14, 2015
Is IVF-served two different ways-more cost-effective than IUI with controlled ovarian hyperstimulation?R I Tjon-Kon-Fat, A J Bensdorp, P M M Bossuyt, et al.
European Geriatric Medicine|February 7, 2023
Atypical presentation of COVID-19 in older patients is associated with frailty but not with adverse outcomesJoy E van Son, Elisabeth C P Kahn, Jessica M van der Bol, et al.
Pageof 75

Showing results (691-700 of 743) with videos related to

Sort By:
Pageof 75
Clinical Epigenetics|November 6, 2019
A genome-wide DNA methylation signature for SETD1B-related syndromeI M Krzyzewska, S M Maas, P Henneman, et al.
Hypertension (Dallas, Tex. : 1979)|July 9, 2020
Pregnancy-Related Complications in Patients With Fibromuscular Dysplasia: A Report From the European/International Fibromuscular Dysplasia RegistryMarco Pappaccogli, Aleksander Prejbisz, Simina Ciurică, et al.
BMC Cancer|August 20, 2015
Early salpingectomy (TUbectomy) with delayed oophorectomy to improve quality of life as alternative for risk-reducing salpingo-oophorectomy in BRCA1/2 mutation carriers (TUBA study): a prospective non-randomised multicentre studyMarline G Harmsen, Marieke Arts-de Jong, Nicoline Hoogerbrugge, et al.
Human Genetics|December 12, 2013
X-linked congenital ptosis and associated intellectual disability, short stature, microcephaly, cleft palate, digital and genital abnormalities define novel Xq25q26 duplication syndromeR S Møller, L R Jensen, S M Maas, et al.
American Journal of Human Genetics|November 24, 2020
Heterozygous Variants in KDM4B Lead to Global Developmental Delay and Neuroanatomical DefectsAnna R Duncan, Antonio Vitobello, Stephan C Collins, et al.
European Journal of Human Genetics : EJHG|March 31, 2025
DDX3X-related neurodevelopmental disorder in males - presenting a new cohort of 19 males and a literature reviewMilou G P Kennis, Dmitrijs Rots, Arjan Bouman, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 8, 2026
Clinical, Genetic, and Imaging Characteristics of SCA27B: Insights from a Large Dutch CohortTeije H van Prooije, Maartje Pennings, Roderick P P W M Maas, et al.
Clinical Epigenetics|August 1, 2024
Multi-locus imprinting disturbance (MLID): interim joint statement for clinical and molecular diagnosisDeborah J G Mackay, Gabriella Gazdagh, David Monk, et al.
Human Reproduction (Oxford, England)|August 14, 2015
Is IVF-served two different ways-more cost-effective than IUI with controlled ovarian hyperstimulation?R I Tjon-Kon-Fat, A J Bensdorp, P M M Bossuyt, et al.
European Geriatric Medicine|February 7, 2023
Atypical presentation of COVID-19 in older patients is associated with frailty but not with adverse outcomesJoy E van Son, Elisabeth C P Kahn, Jessica M van der Bol, et al.
Pageof 75