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

Jeroen Breckpot

Showing results (1-10 of 103) with videos related to

Pageof 11
Sort By:
Journal of Speech, Language, and Hearing Research : JSLHR|October 17, 2024
Language Profiles of School-Age Children With 16p11.2 Copy Number Variants in a Clinically Ascertained CohortJente Verbesselt, Jeroen Breckpot, Inge Zink, et al.
American Journal of Medical Genetics. Part A|September 7, 2021
Cross-sectional and longitudinal findings in patients with proximal 22q11.2 duplication: A retrospective chart studyJente Verbesselt, Inge Zink, Jeroen Breckpot, et al.
Journal of Neurodevelopmental Disorders|June 19, 2025
Developmental milestones and cognitive trajectories in school-aged children with 16p11.2 deletionJente Verbesselt, Jeroen Breckpot, Inge Zink, et al.
Journal of Endocrinological Investigation|November 28, 2024
Management of autosomal dominant hypocalcemia type 1: Literature review and clinical practice recommendationsThomas De Coster, Karel David, Jeroen Breckpot, et al.
Scientific Reports|November 10, 2020
Centrosome and ciliary abnormalities in fetal akinesia deformation sequence human fibroblastsRamona Jühlen, Valérie Martinelli, Chiara Vinci, et al.
Calcified Tissue International|April 20, 2020
A Case of a Heterozygous Inactivating CASR Variant with Adult-Onset Symptomatic Hypercalcemia Requiring Extensive SurgeryLaurens Veldeman, Saskia Robbrecht, Jeroen Breckpot, et al.
American Journal of Medical Genetics. Part A|August 21, 2007
A microduplication of CBP in a patient with mental retardation and a congenital heart defectBernard Thienpont, Jeroen Breckpot, Maureen Holvoet, et al.
European Journal of Medical Genetics|February 20, 2008
A complex submicroscopic chromosomal imbalance in 19p13.11 with one microduplication and two microtriplicationsBernard Thienpont, Jeroen Breckpot, Joris R Vermeesch, et al.
Genes|October 27, 2022
Parent-Reported Social-Communicative Skills of Children with 22q11.2 Copy Number Variants and SiblingsJente Verbesselt, Ellen Van Den Heuvel, Jeroen Breckpot, et al.
European Journal of Medical Genetics|September 4, 2010
Duplication of the TGFBR1 gene causes features of Loeys-Dietz syndromeJeroen Breckpot, Werner Budts, Francis De Zegher, et al.
Pageof 11

Showing results (1-10 of 103) with videos related to

Sort By:
Pageof 11
Journal of Speech, Language, and Hearing Research : JSLHR|October 17, 2024
Language Profiles of School-Age Children With 16p11.2 Copy Number Variants in a Clinically Ascertained CohortJente Verbesselt, Jeroen Breckpot, Inge Zink, et al.
American Journal of Medical Genetics. Part A|September 7, 2021
Cross-sectional and longitudinal findings in patients with proximal 22q11.2 duplication: A retrospective chart studyJente Verbesselt, Inge Zink, Jeroen Breckpot, et al.
Journal of Neurodevelopmental Disorders|June 19, 2025
Developmental milestones and cognitive trajectories in school-aged children with 16p11.2 deletionJente Verbesselt, Jeroen Breckpot, Inge Zink, et al.
Journal of Endocrinological Investigation|November 28, 2024
Management of autosomal dominant hypocalcemia type 1: Literature review and clinical practice recommendationsThomas De Coster, Karel David, Jeroen Breckpot, et al.
Scientific Reports|November 10, 2020
Centrosome and ciliary abnormalities in fetal akinesia deformation sequence human fibroblastsRamona Jühlen, Valérie Martinelli, Chiara Vinci, et al.
Calcified Tissue International|April 20, 2020
A Case of a Heterozygous Inactivating CASR Variant with Adult-Onset Symptomatic Hypercalcemia Requiring Extensive SurgeryLaurens Veldeman, Saskia Robbrecht, Jeroen Breckpot, et al.
American Journal of Medical Genetics. Part A|August 21, 2007
A microduplication of CBP in a patient with mental retardation and a congenital heart defectBernard Thienpont, Jeroen Breckpot, Maureen Holvoet, et al.
European Journal of Medical Genetics|February 20, 2008
A complex submicroscopic chromosomal imbalance in 19p13.11 with one microduplication and two microtriplicationsBernard Thienpont, Jeroen Breckpot, Joris R Vermeesch, et al.
Genes|October 27, 2022
Parent-Reported Social-Communicative Skills of Children with 22q11.2 Copy Number Variants and SiblingsJente Verbesselt, Ellen Van Den Heuvel, Jeroen Breckpot, et al.
European Journal of Medical Genetics|September 4, 2010
Duplication of the TGFBR1 gene causes features of Loeys-Dietz syndromeJeroen Breckpot, Werner Budts, Francis De Zegher, et al.
Pageof 11