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Hilde Peeters

Showing results (41-50 of 99) with videos related to

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American Journal of Medical Genetics. Part A|September 9, 2017
Testing the face shape hypothesis in twins discordant for nonsyndromic orofacial cleftingJasmien Roosenboom, Karlijne Indencleef, Greet Hens, et al.
European Journal of Human Genetics : EJHG|June 10, 2011
Haploinsufficiency of ANKRD11 causes mild cognitive impairment, short stature and minor dysmorphismsMala Isrie, Yvonne Hendriks, Nicole Gielissen, et al.
Journal of Neurodevelopmental Disorders|November 28, 2025
The importance of intrafamilial cognitive phenotyping by the case of 22q11.2 deletion, 15q11.2 deletion, and families with inherited copy number variants of unknown significanceElise Pelgrims, Laurens Hannes, Ilse Noens, et al.
Frontiers in Genetics|December 5, 2018
Spatially Dense 3D Facial Heritability and Modules of Co-heritability in a Father-Offspring DesignHanne Hoskens, Jiarui Li, Karlijne Indencleef, et al.
European Journal of Human Genetics : EJHG|May 18, 2017
Variants in TTC25 affect autistic trait in patients with autism spectrum disorder and general populationDina Vojinovic, Nathalie Brison, Shahzad Ahmad, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 20, 2014
Association of CDH11 with non-syndromic ASDAn Crepel, Veerle De Wolf, Nathalie Brison, et al.
American Journal of Medical Genetics. Part A|October 23, 2018
Olfactory function in patients with nonsyndromic orofacial clefts and their unaffected relativesJasmien Roosenboom, Robert Hermans, Frederik Lammens, et al.
Journal of Medical Genetics|July 20, 2022
Refining nosology by modelling variation among facial phenotypes: the RASopathiesHarold Matthews, Michiel Vanneste, Kaitlin Katsura, et al.
Genome Medicine|January 9, 2025
Clinical evaluation of long-read sequencing-based episignature detection in developmental disordersMathilde Geysens, Benjamin Huremagic, Erika Souche, et al.
The Journal of Pediatrics|February 9, 2010
Array comparative genomic hybridization as a diagnostic tool for syndromic heart defectsJeroen Breckpot, Bernard Thienpont, Hilde Peeters, et al.
Pageof 10

Showing results (41-50 of 99) with videos related to

Sort By:
Pageof 10
American Journal of Medical Genetics. Part A|September 9, 2017
Testing the face shape hypothesis in twins discordant for nonsyndromic orofacial cleftingJasmien Roosenboom, Karlijne Indencleef, Greet Hens, et al.
European Journal of Human Genetics : EJHG|June 10, 2011
Haploinsufficiency of ANKRD11 causes mild cognitive impairment, short stature and minor dysmorphismsMala Isrie, Yvonne Hendriks, Nicole Gielissen, et al.
Journal of Neurodevelopmental Disorders|November 28, 2025
The importance of intrafamilial cognitive phenotyping by the case of 22q11.2 deletion, 15q11.2 deletion, and families with inherited copy number variants of unknown significanceElise Pelgrims, Laurens Hannes, Ilse Noens, et al.
Frontiers in Genetics|December 5, 2018
Spatially Dense 3D Facial Heritability and Modules of Co-heritability in a Father-Offspring DesignHanne Hoskens, Jiarui Li, Karlijne Indencleef, et al.
European Journal of Human Genetics : EJHG|May 18, 2017
Variants in TTC25 affect autistic trait in patients with autism spectrum disorder and general populationDina Vojinovic, Nathalie Brison, Shahzad Ahmad, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 20, 2014
Association of CDH11 with non-syndromic ASDAn Crepel, Veerle De Wolf, Nathalie Brison, et al.
American Journal of Medical Genetics. Part A|October 23, 2018
Olfactory function in patients with nonsyndromic orofacial clefts and their unaffected relativesJasmien Roosenboom, Robert Hermans, Frederik Lammens, et al.
Journal of Medical Genetics|July 20, 2022
Refining nosology by modelling variation among facial phenotypes: the RASopathiesHarold Matthews, Michiel Vanneste, Kaitlin Katsura, et al.
Genome Medicine|January 9, 2025
Clinical evaluation of long-read sequencing-based episignature detection in developmental disordersMathilde Geysens, Benjamin Huremagic, Erika Souche, et al.
The Journal of Pediatrics|February 9, 2010
Array comparative genomic hybridization as a diagnostic tool for syndromic heart defectsJeroen Breckpot, Bernard Thienpont, Hilde Peeters, et al.
Pageof 10