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 (41-50 of 103) with videos related to

Pageof 11
Sort By:
European Journal of Human Genetics : EJHG|May 7, 2015
Chromosome 22q12.1 microdeletions: confirmation of the MN1 gene as a candidate gene for cleft palateJeroen Breckpot, Britt-Marie Anderlid, Yasemin Alanay, et al.
Heart (British Cardiac Society)|July 13, 2026
Causes of congenital heart disease: an integrative narrative reviewHuimin Su, Julie De Backer, Jeroen Breckpot, et al.
American Journal of Human Genetics|October 3, 2017
Nested Inversion Polymorphisms Predispose Chromosome 22q11.2 to Meiotic RearrangementsWolfram Demaerel, Matthew S Hestand, Elfi Vergaelen, et al.
European Journal of Medical Genetics|February 15, 2020
Next-generation sequencing in prenatal setting: Some examples of unexpected variant associationBerardo Rinaldi, Valerie Race, Anniek Corveleyn, et al.
Biorxiv : the Preprint Server for Biology|April 2, 2024
Multiple paralogues and recombination mechanisms drive the high incidence of 22q11.2 Deletion SyndromeLisanne Vervoort, Nicolas Dierckxsens, Marta Sousa Santos, et al.
Genome Research|November 13, 2024
Multiple paralogs and recombination mechanisms contribute to the high incidence of 22q11.2 deletion syndromeLisanne Vervoort, Nicolas Dierckxsens, Marta Sousa Santos, et al.
Journal of Medical Genetics|January 15, 2020
The clinical relevance of intragenic <i>NRXN1</i> deletionsNele Cosemans, Laura Vandenhove, Annick Vogels, et al.
European Journal of Human Genetics : EJHG|July 27, 2022
Rare autosomal trisomies detected by non-invasive prenatal testing: an overview of current knowledgeLore Lannoo, Khaila van Straaten, Jeroen Breckpot, et al.
American Journal of Human Genetics|May 25, 2010
Haploinsufficiency of TAB2 causes congenital heart defects in humansBernard Thienpont, Litu Zhang, Alex V Postma, et al.
European Journal of Human Genetics : EJHG|June 16, 2018
Phenotypic spectrum of Au-Kline syndrome: a report of six new cases and review of the literatureP Y Billie Au, Caitlin Goedhart, Marcia Ferguson, et al.
Pageof 11

Showing results (41-50 of 103) with videos related to

Sort By:
Pageof 11
European Journal of Human Genetics : EJHG|May 7, 2015
Chromosome 22q12.1 microdeletions: confirmation of the MN1 gene as a candidate gene for cleft palateJeroen Breckpot, Britt-Marie Anderlid, Yasemin Alanay, et al.
Heart (British Cardiac Society)|July 13, 2026
Causes of congenital heart disease: an integrative narrative reviewHuimin Su, Julie De Backer, Jeroen Breckpot, et al.
American Journal of Human Genetics|October 3, 2017
Nested Inversion Polymorphisms Predispose Chromosome 22q11.2 to Meiotic RearrangementsWolfram Demaerel, Matthew S Hestand, Elfi Vergaelen, et al.
European Journal of Medical Genetics|February 15, 2020
Next-generation sequencing in prenatal setting: Some examples of unexpected variant associationBerardo Rinaldi, Valerie Race, Anniek Corveleyn, et al.
Biorxiv : the Preprint Server for Biology|April 2, 2024
Multiple paralogues and recombination mechanisms drive the high incidence of 22q11.2 Deletion SyndromeLisanne Vervoort, Nicolas Dierckxsens, Marta Sousa Santos, et al.
Genome Research|November 13, 2024
Multiple paralogs and recombination mechanisms contribute to the high incidence of 22q11.2 deletion syndromeLisanne Vervoort, Nicolas Dierckxsens, Marta Sousa Santos, et al.
Journal of Medical Genetics|January 15, 2020
The clinical relevance of intragenic <i>NRXN1</i> deletionsNele Cosemans, Laura Vandenhove, Annick Vogels, et al.
European Journal of Human Genetics : EJHG|July 27, 2022
Rare autosomal trisomies detected by non-invasive prenatal testing: an overview of current knowledgeLore Lannoo, Khaila van Straaten, Jeroen Breckpot, et al.
American Journal of Human Genetics|May 25, 2010
Haploinsufficiency of TAB2 causes congenital heart defects in humansBernard Thienpont, Litu Zhang, Alex V Postma, et al.
European Journal of Human Genetics : EJHG|June 16, 2018
Phenotypic spectrum of Au-Kline syndrome: a report of six new cases and review of the literatureP Y Billie Au, Caitlin Goedhart, Marcia Ferguson, et al.
Pageof 11