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Koen Devriendt

Showing results (41-50 of 183) with videos related to

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European Journal of Medical Genetics|January 26, 2011
Circumferential skin creases, cleft palate, typical face, intellectual disability and growth delay: "circumferential skin creases Kunze type"Leen Wouters, Celia Maria Rodriguez Rodriguez, Elena Porta Dapena, et al.
European Journal of Medical Genetics|January 26, 2023
NID1-related autosomal dominant Dandy-Walker malformation with occipital cephalocele in three generationsSofie Dietvorst, Koen Devriendt, Julie Lambert, et al.
European Journal of Human Genetics : EJHG|August 10, 2006
A novel CSX/NKX2-5 mutation causes autosomal-dominant AV block: are atrial fibrillation and syncopes part of the phenotype?Ilse Gutierrez-Roelens, Luc De Roy, Caroline Ovaert, et al.
Human Mutation|August 31, 2002
Human piebaldism: six novel mutations of the proto-oncogene KITPetros Syrris, Kirsten Heathcote, Romeo Carrozzo, et al.
Genetic Testing|April 29, 2005
Predictive testing for hereditary nonpolyposis colorectal cancer: subjective perception regarding colorectal and endometrial cancer, distress, and health-related behavior at one year post-testErna Claes, Lieve Denayer, Gerry Evers-Kiebooms, et al.
European Journal of Human Genetics : EJHG|December 18, 2003
Minimum prevalence, birth incidence and cause of death for Prader-Willi syndrome in FlandersAnnick Vogels, Jenneke Van Den Ende, Kathelijne Keymolen, et al.
Developmental Medicine and Child Neurology|November 18, 2005
Early motor development in young children with 22q.11 deletion syndrome and a conotruncal heart defectAnn Swillen, Hilde Feys, Tamara Adriaens, et al.
Prenatal Diagnosis|December 15, 2017
Maternal liver transplant: Another cause of discordant fetal sex determination using cell-free DNAMaria Neofytou, Nathalie Brison, Kris Van den Bogaert, et al.
Journal of Medical Genetics|July 9, 2010
Genomic rearrangements of the GREM1-FMN1 locus cause oligosyndactyly, radio-ulnar synostosis, hearing loss, renal defects syndrome and Cenani--Lenz-like non-syndromic oligosyndactylyBoyan Ivanov Dimitrov, Thierry Voet, Luc De Smet, et al.
Child Neuropsychology : a Journal on Normal and Abnormal Development in Childhood and Adolescence|April 13, 2005
Atypical neuropsychological profile in a boy with 22q11.2 Deletion SyndromePeter Stiers, Ann Swillen, Bert De Smedt, et al.
Pageof 19

Showing results (41-50 of 183) with videos related to

Sort By:
Pageof 19
European Journal of Medical Genetics|January 26, 2011
Circumferential skin creases, cleft palate, typical face, intellectual disability and growth delay: "circumferential skin creases Kunze type"Leen Wouters, Celia Maria Rodriguez Rodriguez, Elena Porta Dapena, et al.
European Journal of Medical Genetics|January 26, 2023
NID1-related autosomal dominant Dandy-Walker malformation with occipital cephalocele in three generationsSofie Dietvorst, Koen Devriendt, Julie Lambert, et al.
European Journal of Human Genetics : EJHG|August 10, 2006
A novel CSX/NKX2-5 mutation causes autosomal-dominant AV block: are atrial fibrillation and syncopes part of the phenotype?Ilse Gutierrez-Roelens, Luc De Roy, Caroline Ovaert, et al.
Human Mutation|August 31, 2002
Human piebaldism: six novel mutations of the proto-oncogene KITPetros Syrris, Kirsten Heathcote, Romeo Carrozzo, et al.
Genetic Testing|April 29, 2005
Predictive testing for hereditary nonpolyposis colorectal cancer: subjective perception regarding colorectal and endometrial cancer, distress, and health-related behavior at one year post-testErna Claes, Lieve Denayer, Gerry Evers-Kiebooms, et al.
European Journal of Human Genetics : EJHG|December 18, 2003
Minimum prevalence, birth incidence and cause of death for Prader-Willi syndrome in FlandersAnnick Vogels, Jenneke Van Den Ende, Kathelijne Keymolen, et al.
Developmental Medicine and Child Neurology|November 18, 2005
Early motor development in young children with 22q.11 deletion syndrome and a conotruncal heart defectAnn Swillen, Hilde Feys, Tamara Adriaens, et al.
Prenatal Diagnosis|December 15, 2017
Maternal liver transplant: Another cause of discordant fetal sex determination using cell-free DNAMaria Neofytou, Nathalie Brison, Kris Van den Bogaert, et al.
Journal of Medical Genetics|July 9, 2010
Genomic rearrangements of the GREM1-FMN1 locus cause oligosyndactyly, radio-ulnar synostosis, hearing loss, renal defects syndrome and Cenani--Lenz-like non-syndromic oligosyndactylyBoyan Ivanov Dimitrov, Thierry Voet, Luc De Smet, et al.
Child Neuropsychology : a Journal on Normal and Abnormal Development in Childhood and Adolescence|April 13, 2005
Atypical neuropsychological profile in a boy with 22q11.2 Deletion SyndromePeter Stiers, Ann Swillen, Bert De Smedt, et al.
Pageof 19