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Koenraad Devriendt

Showing results (21-30 of 190) with videos related to

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European Journal of Pediatrics|August 21, 2007
Ocular findings in children with a microdeletion in chromosome 22q11.2Ingele Casteels, Patricia Casaer, Marc Gewillig, et al.
Annals of Human Genetics|May 15, 2025
Automated Evaluation of D-Score for Facial Dysmorphism Analysis in Central African Children With Developmental DisordersPrince Makay, Gerrye Mubungu, Prosper Lukusa Tshilobo, et al.
Strabismus|October 28, 2021
Extraocular muscle hypoplasia associated with Axenfeld-Rieger syndromeMilo De Decker, Catherine Cassiman, Ingele Casteels, et al.
Clinical Dysmorphology|February 27, 2010
Congenital nasal piriform aperture stenosis as a rare manifestation of monosomy 1p36Jeroen Breckpot, Robert Hermans, Vincent Vander Poorten, et al.
American Journal of Medical Genetics. Part A|March 13, 2026
Differentiating the Clinical and Variant Spectrum of Hardikar Syndrome From Other MED12-Related Developmental DisordersTinne Warmoeskerken, Miel Theunis, Kris Van den Bogaert, et al.
Genomics|April 12, 2005
Defining a holoprosencephaly locus on human chromosome 14q13 and characterization of potential candidate genesDeepak Kamnasaran, Chih-Ping Chen, Koenraad Devriendt, 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.
European Journal of Human Genetics : EJHG|May 19, 2011
The causality of de novo copy number variants is overestimatedJoris R Vermeesch, Irina Balikova, Connie Schrander-Stumpel, et al.
Clinical Dysmorphology|August 24, 2018
Congenital lateral abdominal wall defect in two Congolese childrenGerrye Mubungu, Bertin Kadima, Aimé Lumaka, et al.
American Journal of Medical Genetics. Part A|February 26, 2015
MEIS2 involvement in cardiac development, cleft palate, and intellectual disabilityJacoba J Louw, Anniek Corveleyn, Yaojuan Jia, et al.
Pageof 19

Showing results (21-30 of 190) with videos related to

Sort By:
Pageof 19
European Journal of Pediatrics|August 21, 2007
Ocular findings in children with a microdeletion in chromosome 22q11.2Ingele Casteels, Patricia Casaer, Marc Gewillig, et al.
Annals of Human Genetics|May 15, 2025
Automated Evaluation of D-Score for Facial Dysmorphism Analysis in Central African Children With Developmental DisordersPrince Makay, Gerrye Mubungu, Prosper Lukusa Tshilobo, et al.
Strabismus|October 28, 2021
Extraocular muscle hypoplasia associated with Axenfeld-Rieger syndromeMilo De Decker, Catherine Cassiman, Ingele Casteels, et al.
Clinical Dysmorphology|February 27, 2010
Congenital nasal piriform aperture stenosis as a rare manifestation of monosomy 1p36Jeroen Breckpot, Robert Hermans, Vincent Vander Poorten, et al.
American Journal of Medical Genetics. Part A|March 13, 2026
Differentiating the Clinical and Variant Spectrum of Hardikar Syndrome From Other MED12-Related Developmental DisordersTinne Warmoeskerken, Miel Theunis, Kris Van den Bogaert, et al.
Genomics|April 12, 2005
Defining a holoprosencephaly locus on human chromosome 14q13 and characterization of potential candidate genesDeepak Kamnasaran, Chih-Ping Chen, Koenraad Devriendt, 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.
European Journal of Human Genetics : EJHG|May 19, 2011
The causality of de novo copy number variants is overestimatedJoris R Vermeesch, Irina Balikova, Connie Schrander-Stumpel, et al.
Clinical Dysmorphology|August 24, 2018
Congenital lateral abdominal wall defect in two Congolese childrenGerrye Mubungu, Bertin Kadima, Aimé Lumaka, et al.
American Journal of Medical Genetics. Part A|February 26, 2015
MEIS2 involvement in cardiac development, cleft palate, and intellectual disabilityJacoba J Louw, Anniek Corveleyn, Yaojuan Jia, et al.
Pageof 19