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Hilde Peeters

Showing results (71-80 of 99) with videos related to

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Biorxiv : the Preprint Server for Biology|April 2, 2024
Multiple paralogues and recombination mechanisms drive the high incidence of 22q11.2 Deletion SyndromeLisanne Vervoort, Nicolas Dierckxsens, Marta Sousa Santos, et al.
Nature Communications|December 2, 2024
Syndrome-informed phenotyping identifies a polygenic background for achondroplasia-like facial variation in the general populationMichiel Vanneste, Hanne Hoskens, Seppe Goovaerts, et al.
Genome Research|November 13, 2024
Multiple paralogs and recombination mechanisms contribute to the high incidence of 22q11.2 deletion syndromeLisanne Vervoort, Nicolas Dierckxsens, Marta Sousa Santos, et al.
European Journal of Human Genetics : EJHG|July 27, 2022
Rare autosomal trisomies detected by non-invasive prenatal testing: an overview of current knowledgeLore Lannoo, Khaila van Straaten, Jeroen Breckpot, et al.
Scientific Reports|June 10, 2021
Large-scale open-source three-dimensional growth curves for clinical facial assessment and objective description of facial dysmorphismHarold S Matthews, Richard L Palmer, Gareth S Baynam, et al.
Molecular & Cellular Proteomics : MCP|October 27, 2010
Human plasma glycome in attention-deficit hyperactivity disorder and autism spectrum disordersNela Pivac, Ana Knezević, Olga Gornik, et al.
European Journal of Human Genetics : EJHG|January 15, 2015
Noninvasive prenatal testing using a novel analysis pipeline to screen for all autosomal fetal aneuploidies improves pregnancy managementBaran Bayindir, Luc Dehaspe, Nathalie Brison, et al.
Plos Genetics|May 13, 2021
3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologiesHanne Hoskens, Dongjing Liu, Sahin Naqvi, et al.
Nature Genetics|April 6, 2021
Shared heritability of human face and brain shapeSahin Naqvi, Yoeri Sleyp, Hanne Hoskens, et al.
Molecular Autism|January 2, 2020
Increased Ca<sup>2+</sup> signaling in <i>NRXN1α</i><sup></sup> neurons derived from ASD induced pluripotent stem cellsSahar Avazzadeh, Katya McDonagh, Jamie Reilly, et al.
Pageof 10

Showing results (71-80 of 99) with videos related to

Sort By:
Pageof 10
Biorxiv : the Preprint Server for Biology|April 2, 2024
Multiple paralogues and recombination mechanisms drive the high incidence of 22q11.2 Deletion SyndromeLisanne Vervoort, Nicolas Dierckxsens, Marta Sousa Santos, et al.
Nature Communications|December 2, 2024
Syndrome-informed phenotyping identifies a polygenic background for achondroplasia-like facial variation in the general populationMichiel Vanneste, Hanne Hoskens, Seppe Goovaerts, et al.
Genome Research|November 13, 2024
Multiple paralogs and recombination mechanisms contribute to the high incidence of 22q11.2 deletion syndromeLisanne Vervoort, Nicolas Dierckxsens, Marta Sousa Santos, et al.
European Journal of Human Genetics : EJHG|July 27, 2022
Rare autosomal trisomies detected by non-invasive prenatal testing: an overview of current knowledgeLore Lannoo, Khaila van Straaten, Jeroen Breckpot, et al.
Scientific Reports|June 10, 2021
Large-scale open-source three-dimensional growth curves for clinical facial assessment and objective description of facial dysmorphismHarold S Matthews, Richard L Palmer, Gareth S Baynam, et al.
Molecular & Cellular Proteomics : MCP|October 27, 2010
Human plasma glycome in attention-deficit hyperactivity disorder and autism spectrum disordersNela Pivac, Ana Knezević, Olga Gornik, et al.
European Journal of Human Genetics : EJHG|January 15, 2015
Noninvasive prenatal testing using a novel analysis pipeline to screen for all autosomal fetal aneuploidies improves pregnancy managementBaran Bayindir, Luc Dehaspe, Nathalie Brison, et al.
Plos Genetics|May 13, 2021
3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologiesHanne Hoskens, Dongjing Liu, Sahin Naqvi, et al.
Nature Genetics|April 6, 2021
Shared heritability of human face and brain shapeSahin Naqvi, Yoeri Sleyp, Hanne Hoskens, et al.
Molecular Autism|January 2, 2020
Increased Ca<sup>2+</sup> signaling in <i>NRXN1α</i><sup></sup> neurons derived from ASD induced pluripotent stem cellsSahar Avazzadeh, Katya McDonagh, Jamie Reilly, et al.
Pageof 10