Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Tjitske Kleefstra

Showing results (1-10 of 234) with videos related to

Pageof 24
Sort By:
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|October 3, 2007
The chromosome 9q subtelomere deletion syndromeDouglas R Stewart, Tjitske Kleefstra
Nederlands Tijdschrift Voor Geneeskunde|November 20, 2014
[Genetic diagnostics in intellectual disability: what is the benefit?]Marjolein H Willemsen, Tjitske Kleefstra
European Journal of Medical Genetics|March 28, 2009
Emerging microdeletion and microduplication syndromes; the counseling paradigmConny M A van Ravenswaaij-Arts, Tjitske Kleefstra
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|July 31, 2009
Behavioral phenotype in the 9q subtelomeric deletion syndrome: a report about two adult patientsWillem M A Verhoeven, Tjitske Kleefstra, Jos I M Egger
Neuropharmacology|January 18, 2014
The genetics of cognitive epigeneticsTjitske Kleefstra, Annette Schenck, Jamie M Kramer, et al.
Frontiers in Genetics|December 20, 2023
Editorial: Characterizing the neurobehavioral phenotype of mendelian disorders of epigenetic machineryRowena Ng, Jacqueline Harris, Tjitske Kleefstra, et al.
European Journal of Medical Genetics|July 16, 2013
Clinical delineation of a patient with trisomy 12q23q24Arjan Bouman, Anke Schuitema, Rolph Pfundt, et al.
European Journal of Medical Genetics|August 19, 2025
Parental experiences and needs in Kleefstra Syndrome: A semi-structured interview studySietske A L van Till, Arianne Bouman, Tjitske Kleefstra, et al.
Neuropsychiatric Disease and Treatment|June 9, 2016
Absence epilepsy and the CHD2 gene: an adolescent male with moderate intellectual disability, short-lasting psychoses, and an interstitial deletion in 15q26.1-q26.2Willem Ma Verhoeven, Jos Im Egger, Alida C Knegt, et al.
Frontiers in Immunology|April 13, 2026
Clinical immunology in chromatinopathies: a scoping reviewDieke Jans, Burcu Al, Arianne Bouman, et al.
Pageof 24

Showing results (1-10 of 234) with videos related to

Sort By:
Pageof 24
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|October 3, 2007
The chromosome 9q subtelomere deletion syndromeDouglas R Stewart, Tjitske Kleefstra
Nederlands Tijdschrift Voor Geneeskunde|November 20, 2014
[Genetic diagnostics in intellectual disability: what is the benefit?]Marjolein H Willemsen, Tjitske Kleefstra
European Journal of Medical Genetics|March 28, 2009
Emerging microdeletion and microduplication syndromes; the counseling paradigmConny M A van Ravenswaaij-Arts, Tjitske Kleefstra
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|July 31, 2009
Behavioral phenotype in the 9q subtelomeric deletion syndrome: a report about two adult patientsWillem M A Verhoeven, Tjitske Kleefstra, Jos I M Egger
Neuropharmacology|January 18, 2014
The genetics of cognitive epigeneticsTjitske Kleefstra, Annette Schenck, Jamie M Kramer, et al.
Frontiers in Genetics|December 20, 2023
Editorial: Characterizing the neurobehavioral phenotype of mendelian disorders of epigenetic machineryRowena Ng, Jacqueline Harris, Tjitske Kleefstra, et al.
European Journal of Medical Genetics|July 16, 2013
Clinical delineation of a patient with trisomy 12q23q24Arjan Bouman, Anke Schuitema, Rolph Pfundt, et al.
European Journal of Medical Genetics|August 19, 2025
Parental experiences and needs in Kleefstra Syndrome: A semi-structured interview studySietske A L van Till, Arianne Bouman, Tjitske Kleefstra, et al.
Neuropsychiatric Disease and Treatment|June 9, 2016
Absence epilepsy and the CHD2 gene: an adolescent male with moderate intellectual disability, short-lasting psychoses, and an interstitial deletion in 15q26.1-q26.2Willem Ma Verhoeven, Jos Im Egger, Alida C Knegt, et al.
Frontiers in Immunology|April 13, 2026
Clinical immunology in chromatinopathies: a scoping reviewDieke Jans, Burcu Al, Arianne Bouman, et al.
Pageof 24