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Hilde Peeters

Showing results (31-40 of 99) with videos related to

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European Journal of Medical Genetics|March 1, 2015
Homozygous missense mutation in STYXL1 associated with moderate intellectual disability, epilepsy and behavioural complexitiesMala Isrie, Masoud Zamani Esteki, Hilde Peeters, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|September 10, 2019
The East Flanders Prospective Twin Survey (EFPTS): 55 Years LaterCatherine Derom, Evert Thiery, Bart P F Rutten, et al.
Personalized Medicine|June 4, 2021
Expanded carrier screening in Flanders (Belgium): an online survey on the perspectives of nonpregnant reproductive-aged womenEva Van Steijvoort, Heleen Devolder, Inne Geysen, et al.
Scientific Reports|January 3, 2025
Analysis and prediction of condylar resorption following orthognathic surgeryPieter-Jan Verhelst, Sigrid Janssens, Harold Matthews, et al.
European Journal of Medical Genetics|June 28, 2014
Homozygous loss-of-function mutation in ALMS1 causes the lethal disorder mitogenic cardiomyopathy in two siblingsJacoba J Louw, Anniek Corveleyn, Yaojuan Jia, et al.
Molecular Autism|October 27, 2015
Platelet studies in autism spectrum disorder patients and first-degree relativesNora Bijl, Chantal Thys, Christine Wittevrongel, 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.
European Journal of Medical Genetics|February 11, 2018
ZNF462 and KLF12 are disrupted by a de novo translocation in a patient with syndromic intellectual disability and autism spectrum disorderNele Cosemans, Laura Vandenhove, Jarymke Maljaars, 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.
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.
Pageof 10

Showing results (31-40 of 99) with videos related to

Sort By:
Pageof 10
European Journal of Medical Genetics|March 1, 2015
Homozygous missense mutation in STYXL1 associated with moderate intellectual disability, epilepsy and behavioural complexitiesMala Isrie, Masoud Zamani Esteki, Hilde Peeters, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|September 10, 2019
The East Flanders Prospective Twin Survey (EFPTS): 55 Years LaterCatherine Derom, Evert Thiery, Bart P F Rutten, et al.
Personalized Medicine|June 4, 2021
Expanded carrier screening in Flanders (Belgium): an online survey on the perspectives of nonpregnant reproductive-aged womenEva Van Steijvoort, Heleen Devolder, Inne Geysen, et al.
Scientific Reports|January 3, 2025
Analysis and prediction of condylar resorption following orthognathic surgeryPieter-Jan Verhelst, Sigrid Janssens, Harold Matthews, et al.
European Journal of Medical Genetics|June 28, 2014
Homozygous loss-of-function mutation in ALMS1 causes the lethal disorder mitogenic cardiomyopathy in two siblingsJacoba J Louw, Anniek Corveleyn, Yaojuan Jia, et al.
Molecular Autism|October 27, 2015
Platelet studies in autism spectrum disorder patients and first-degree relativesNora Bijl, Chantal Thys, Christine Wittevrongel, 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.
European Journal of Medical Genetics|February 11, 2018
ZNF462 and KLF12 are disrupted by a de novo translocation in a patient with syndromic intellectual disability and autism spectrum disorderNele Cosemans, Laura Vandenhove, Jarymke Maljaars, 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.
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.
Pageof 10