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Koen Devriendt

Showing results (51-60 of 183) with videos related to

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Journal of Children'S Orthopaedics|March 25, 2009
The spectrum of hand and foot malformations in patients with Greig cephalopolysyndactylyPhilippe Debeer, Koen Devriendt, Luc De Smet, et al.
American Journal of Medical Genetics. Part A|May 15, 2012
Variability in expression of a familial 2.79 Mb microdeletion in chromosome 14q22.1-22.2Aimé Lumaka, Christine Van Hole, Ingele Casteels, et al.
Scientific Reports|January 31, 2025
Chromosomal analysis and short-term outcome of prenatally diagnosed congenital heart diseaseMarcellino Verbeke, Laurens Hannes, Koen Devriendt, et al.
Brain & Development|December 27, 2005
MECP2 mutations are an infrequent cause of mental retardation associated with neurological problems in male patientsUte Moog, Kees Van Roozendaal, Eric Smeets, et al.
Neurogenetics|March 8, 2021
8p21.3 deletions are rare causes of non-syndromic autism spectrum disorderNele Cosemans, Jarymke Maljaars, Annick Vogels, et al.
Developmental Medicine and Child Neurology|March 16, 2007
Motor development in school-aged children with 22q11 deletion (velocardiofacial/DiGeorge syndrome)Katrijn Van Aken, Bert De Smedt, Annelies Van Roie, et al.
American Journal of Medical Genetics. Part A|September 27, 2014
A complex Xp11.22 deletion in a patient with syndromic autism: exploration of FAM120C as a positional candidate gene for autismVeerle De Wolf, An Crepel, Frans Schuit, et al.
Clinical Genetics|December 19, 2020
Phenotypic spectrum of the RBM10-mediated intellectual disability and congenital malformation syndrome beyond classic TARP syndrome featuresCandy Kumps, Erika D'haenens, Sarah Vergult, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 9, 2011
Narrowing the critical deletion region for autism spectrum disorders on 16p11.2An Crepel, Jean Steyaert, Wouter De la Marche, et al.
Molecular Genetics & Genomic Medicine|April 27, 2026
Confirmation of Exome Sequencing Results Using Sanger Sequencing-Considerations in a Low-Resource SettingNadja Louw, Samantha Schnell, Mhlekazi Molatoli, et al.
Pageof 19

Showing results (51-60 of 183) with videos related to

Sort By:
Pageof 19
Journal of Children'S Orthopaedics|March 25, 2009
The spectrum of hand and foot malformations in patients with Greig cephalopolysyndactylyPhilippe Debeer, Koen Devriendt, Luc De Smet, et al.
American Journal of Medical Genetics. Part A|May 15, 2012
Variability in expression of a familial 2.79 Mb microdeletion in chromosome 14q22.1-22.2Aimé Lumaka, Christine Van Hole, Ingele Casteels, et al.
Scientific Reports|January 31, 2025
Chromosomal analysis and short-term outcome of prenatally diagnosed congenital heart diseaseMarcellino Verbeke, Laurens Hannes, Koen Devriendt, et al.
Brain & Development|December 27, 2005
MECP2 mutations are an infrequent cause of mental retardation associated with neurological problems in male patientsUte Moog, Kees Van Roozendaal, Eric Smeets, et al.
Neurogenetics|March 8, 2021
8p21.3 deletions are rare causes of non-syndromic autism spectrum disorderNele Cosemans, Jarymke Maljaars, Annick Vogels, et al.
Developmental Medicine and Child Neurology|March 16, 2007
Motor development in school-aged children with 22q11 deletion (velocardiofacial/DiGeorge syndrome)Katrijn Van Aken, Bert De Smedt, Annelies Van Roie, et al.
American Journal of Medical Genetics. Part A|September 27, 2014
A complex Xp11.22 deletion in a patient with syndromic autism: exploration of FAM120C as a positional candidate gene for autismVeerle De Wolf, An Crepel, Frans Schuit, et al.
Clinical Genetics|December 19, 2020
Phenotypic spectrum of the RBM10-mediated intellectual disability and congenital malformation syndrome beyond classic TARP syndrome featuresCandy Kumps, Erika D'haenens, Sarah Vergult, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 9, 2011
Narrowing the critical deletion region for autism spectrum disorders on 16p11.2An Crepel, Jean Steyaert, Wouter De la Marche, et al.
Molecular Genetics & Genomic Medicine|April 27, 2026
Confirmation of Exome Sequencing Results Using Sanger Sequencing-Considerations in a Low-Resource SettingNadja Louw, Samantha Schnell, Mhlekazi Molatoli, et al.
Pageof 19