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

Koenraad Devriendt

Showing results (81-90 of 190) with videos related to

Pageof 19
Sort By:
American Journal of Medical Genetics. Part A|June 17, 2015
Genotypic and phenotypic variation in six patients with solitary median maxillary central incisor syndromeSimon Poelmans, Tatsuro Kawamoto, Francesca Cristofoli, et al.
European Journal of Human Genetics : EJHG|December 20, 2017
Repeat genetic testing with targeted capture sequencing in primary arrhythmia syndrome and cardiomyopathyTomas Robyns, Cuno Kuiperi, Jeroen Breckpot, et al.
American Journal of Medical Genetics. Part A|November 28, 2020
Dysmorphism and major anomalies are a main predictor of survival in newborns admitted to the neonatal intensive care unit in the Democratic Republic of CongoGerrye Mubungu, Prince Makay, Aimé Lumaka, et al.
Journal of Cranio-Maxillo-Facial Surgery : Official Publication of the European Association for Cranio-Maxillo-Facial Surgery|May 27, 2018
Non-syndromic cleft lip and/or cleft palate: Epidemiology and risk factors in Lubumbashi (DR Congo), a case-control studySébastien Mbuyi-Musanzayi, Tony J Kayembe, Marc K Kashal, et al.
Case Reports in Genetics|September 26, 2014
Preaxial polydactyly of the foot: variable expression of trisomy 13 in a case from central AfricaSébastien Mbuyi-Musanzayi, Aimé Lumaka, Bienvenu Yogolelo Asani, et al.
Acta Cardiologica|October 5, 2019
Whole exome sequencing in a large pedigree with DCM identifies a novel mutation in <i>RBM20</i>Tomas Robyns, Rik Willems, Johan Van Cleemput, et al.
American Journal of Medical Genetics. Part A|December 29, 2020
Clinical presentation and evolution of Xia-Gibbs syndrome due to p.Gly375ArgfsTer3 variant in a patient from DR Congo (Central Africa)Gerrye Mubungu, Prince Makay, Bouchra Boujemla, et al.
Frontiers in Genetics|October 20, 2025
A training program to extend the reach of the deciphering developmental disorders in Africa (DDD-Africa) studyAaliah Charles, Zané Lombard, Nadia Carstens, et al.
Clinical Dysmorphology|May 7, 2015
Sacrococcygeal appendage with femur: exoparasitic pyropagus twin, mature teratoma, or disorganization-like syndrome?Sébastien Mbuyi-Musanzayi, Toni Lubala Kasole, Prosper Kalenga Muenze, et al.
European Journal of Medical Genetics|November 10, 2011
BMPR1A is a candidate gene for congenital heart defects associated with the recurrent 10q22q23 deletion syndromeJeroen Breckpot, Léon-Charles Tranchevent, Bernard Thienpont, et al.
Pageof 19

Showing results (81-90 of 190) with videos related to

Sort By:
Pageof 19
American Journal of Medical Genetics. Part A|June 17, 2015
Genotypic and phenotypic variation in six patients with solitary median maxillary central incisor syndromeSimon Poelmans, Tatsuro Kawamoto, Francesca Cristofoli, et al.
European Journal of Human Genetics : EJHG|December 20, 2017
Repeat genetic testing with targeted capture sequencing in primary arrhythmia syndrome and cardiomyopathyTomas Robyns, Cuno Kuiperi, Jeroen Breckpot, et al.
American Journal of Medical Genetics. Part A|November 28, 2020
Dysmorphism and major anomalies are a main predictor of survival in newborns admitted to the neonatal intensive care unit in the Democratic Republic of CongoGerrye Mubungu, Prince Makay, Aimé Lumaka, et al.
Journal of Cranio-Maxillo-Facial Surgery : Official Publication of the European Association for Cranio-Maxillo-Facial Surgery|May 27, 2018
Non-syndromic cleft lip and/or cleft palate: Epidemiology and risk factors in Lubumbashi (DR Congo), a case-control studySébastien Mbuyi-Musanzayi, Tony J Kayembe, Marc K Kashal, et al.
Case Reports in Genetics|September 26, 2014
Preaxial polydactyly of the foot: variable expression of trisomy 13 in a case from central AfricaSébastien Mbuyi-Musanzayi, Aimé Lumaka, Bienvenu Yogolelo Asani, et al.
Acta Cardiologica|October 5, 2019
Whole exome sequencing in a large pedigree with DCM identifies a novel mutation in <i>RBM20</i>Tomas Robyns, Rik Willems, Johan Van Cleemput, et al.
American Journal of Medical Genetics. Part A|December 29, 2020
Clinical presentation and evolution of Xia-Gibbs syndrome due to p.Gly375ArgfsTer3 variant in a patient from DR Congo (Central Africa)Gerrye Mubungu, Prince Makay, Bouchra Boujemla, et al.
Frontiers in Genetics|October 20, 2025
A training program to extend the reach of the deciphering developmental disorders in Africa (DDD-Africa) studyAaliah Charles, Zané Lombard, Nadia Carstens, et al.
Clinical Dysmorphology|May 7, 2015
Sacrococcygeal appendage with femur: exoparasitic pyropagus twin, mature teratoma, or disorganization-like syndrome?Sébastien Mbuyi-Musanzayi, Toni Lubala Kasole, Prosper Kalenga Muenze, et al.
European Journal of Medical Genetics|November 10, 2011
BMPR1A is a candidate gene for congenital heart defects associated with the recurrent 10q22q23 deletion syndromeJeroen Breckpot, Léon-Charles Tranchevent, Bernard Thienpont, et al.
Pageof 19