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Hilde Peeters

Showing results (51-60 of 99) with videos related to

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Genes, Chromosomes & Cancer|May 1, 2013
Multiple pilomatricomas with somatic CTNNB1 mutations in children with constitutive mismatch repair deficiencyMagdalena Chmara, Annekatrin Wernstedt, Bartosz Wasag, et al.
Biorxiv : the Preprint Server for Biology|August 30, 2023
Data-driven trait heritability-based extraction of human facial phenotypesMeng Yuan, Seppe Goovaerts, Hanne Hoskens, et al.
Computer Methods and Programs in Biomedicine|April 21, 2021
3D analysis of facial morphology in Dutch children with cancerFloor A M Postema, Harold Matthews, Saskia M J Hopman, et al.
Plos Genetics|January 23, 2018
Compound heterozygous loss-of-function mutations in KIF20A are associated with a novel lethal congenital cardiomyopathy in two siblingsJacoba J Louw, Ricardo Nunes Bastos, Xiaowen Chen, et al.
Clinical Genetics|July 26, 2024
Toward 3D facial analysis for recognizing Mendelian causes of autism spectrum disorderYoeri Sleyp, Harold S Matthews, Michiel Vanneste, et al.
Briefings in Bioinformatics|March 10, 2025
Optimized phenotyping of complex morphological traits: enhancing discovery of common and rare genetic variantsMeng Yuan, Seppe Goovaerts, Myoung K Lee, et al.
American Journal of Medical Genetics. Part A|August 9, 2018
A comprehensive clinical and genetic study in 127 patients with ID in Kinshasa, DR CongoAimé Lumaka, Valerie Race, Hilde Peeters, et al.
Journal of Child Neurology|September 23, 2015
The Influence of Microdeletions and Microduplications of 16p11.2 on Global Transcription ProfilesMary Kusenda, Vladimir Vacic, Dheeraj Malhotra, et al.
Frontiers in Genetics|November 10, 2018
Six NSCL/P Loci Show Associations With Normal-Range Craniofacial VariationKarlijne Indencleef, Jasmien Roosenboom, Hanne Hoskens, et al.
IEEE Access : Practical Innovations, Open Solutions|August 14, 2025
A 3D Clinical Face Phenotype Space of Genetic Syndromes Using a Triplet-Based Singular Geometric AutoencoderSoha S Mahdi, Eduarda Caldeira, Harold Matthews, et al.
Pageof 10

Showing results (51-60 of 99) with videos related to

Sort By:
Pageof 10
Genes, Chromosomes & Cancer|May 1, 2013
Multiple pilomatricomas with somatic CTNNB1 mutations in children with constitutive mismatch repair deficiencyMagdalena Chmara, Annekatrin Wernstedt, Bartosz Wasag, et al.
Biorxiv : the Preprint Server for Biology|August 30, 2023
Data-driven trait heritability-based extraction of human facial phenotypesMeng Yuan, Seppe Goovaerts, Hanne Hoskens, et al.
Computer Methods and Programs in Biomedicine|April 21, 2021
3D analysis of facial morphology in Dutch children with cancerFloor A M Postema, Harold Matthews, Saskia M J Hopman, et al.
Plos Genetics|January 23, 2018
Compound heterozygous loss-of-function mutations in KIF20A are associated with a novel lethal congenital cardiomyopathy in two siblingsJacoba J Louw, Ricardo Nunes Bastos, Xiaowen Chen, et al.
Clinical Genetics|July 26, 2024
Toward 3D facial analysis for recognizing Mendelian causes of autism spectrum disorderYoeri Sleyp, Harold S Matthews, Michiel Vanneste, et al.
Briefings in Bioinformatics|March 10, 2025
Optimized phenotyping of complex morphological traits: enhancing discovery of common and rare genetic variantsMeng Yuan, Seppe Goovaerts, Myoung K Lee, et al.
American Journal of Medical Genetics. Part A|August 9, 2018
A comprehensive clinical and genetic study in 127 patients with ID in Kinshasa, DR CongoAimé Lumaka, Valerie Race, Hilde Peeters, et al.
Journal of Child Neurology|September 23, 2015
The Influence of Microdeletions and Microduplications of 16p11.2 on Global Transcription ProfilesMary Kusenda, Vladimir Vacic, Dheeraj Malhotra, et al.
Frontiers in Genetics|November 10, 2018
Six NSCL/P Loci Show Associations With Normal-Range Craniofacial VariationKarlijne Indencleef, Jasmien Roosenboom, Hanne Hoskens, et al.
IEEE Access : Practical Innovations, Open Solutions|August 14, 2025
A 3D Clinical Face Phenotype Space of Genetic Syndromes Using a Triplet-Based Singular Geometric AutoencoderSoha S Mahdi, Eduarda Caldeira, Harold Matthews, et al.
Pageof 10