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

Sivagamy Sithambaram

Showing results (1-10 of 7) with videos related to

Pageof 1
Sort By:
Clinical Dysmorphology|August 20, 2015
Inherited duplication of the short arm of chromosome 18p11.32-p11.31 associated with developmental delay/intellectual disabilityMeena Balasubramanian, Sivagamy Sithambaram, Kath Smith
BMJ Case Reports|August 30, 2017
Dilemma of diagnosing sulphonylurea overdose in children: deliberations and considerations before reaching a diagnosisJaya Sujatha Gopal-Kothandapani, Katherine P Wright, Sivagamy Sithambaram, et al.
American Journal of Medical Genetics. Part A|February 15, 2024
PRKACA-related, atrial defects-polydactyly-multiple congenital malformation syndrome in an Indian patientSivagamy Sithambaram, Prince Jacob, Kausthubham Neethukrishna, et al.
The Journal of Craniofacial Surgery|May 25, 2023
Patient Tailored Surgery in Saethre-Chotzen Syndrome: Analysis of Reoperation for Intracranial HypertensionArthur R Kurzbuch, Ben Cooper, Christian Duncan, et al.
European Journal of Human Genetics : EJHG|March 3, 2025
BCL11B-related disease: a single phenotypic entity?J Heather Vedovato-Dos-Santos, Rebecca S Tooze, Sivagamy Sithambaram, et al.
American Journal of Human Genetics|January 14, 2020
Delineation of a Human Mendelian Disorder of the DNA Demethylation Machinery: TET3 DeficiencyDavid B Beck, Ana Petracovici, Chongsheng He, et al.
NPJ Genomic Medicine|November 9, 2021
Deficiency of TET3 leads to a genome-wide DNA hypermethylation episignature in human whole bloodMichael A Levy, David B Beck, Kay Metcalfe, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Clinical Dysmorphology|August 20, 2015
Inherited duplication of the short arm of chromosome 18p11.32-p11.31 associated with developmental delay/intellectual disabilityMeena Balasubramanian, Sivagamy Sithambaram, Kath Smith
BMJ Case Reports|August 30, 2017
Dilemma of diagnosing sulphonylurea overdose in children: deliberations and considerations before reaching a diagnosisJaya Sujatha Gopal-Kothandapani, Katherine P Wright, Sivagamy Sithambaram, et al.
American Journal of Medical Genetics. Part A|February 15, 2024
PRKACA-related, atrial defects-polydactyly-multiple congenital malformation syndrome in an Indian patientSivagamy Sithambaram, Prince Jacob, Kausthubham Neethukrishna, et al.
The Journal of Craniofacial Surgery|May 25, 2023
Patient Tailored Surgery in Saethre-Chotzen Syndrome: Analysis of Reoperation for Intracranial HypertensionArthur R Kurzbuch, Ben Cooper, Christian Duncan, et al.
European Journal of Human Genetics : EJHG|March 3, 2025
BCL11B-related disease: a single phenotypic entity?J Heather Vedovato-Dos-Santos, Rebecca S Tooze, Sivagamy Sithambaram, et al.
American Journal of Human Genetics|January 14, 2020
Delineation of a Human Mendelian Disorder of the DNA Demethylation Machinery: TET3 DeficiencyDavid B Beck, Ana Petracovici, Chongsheng He, et al.
NPJ Genomic Medicine|November 9, 2021
Deficiency of TET3 leads to a genome-wide DNA hypermethylation episignature in human whole bloodMichael A Levy, David B Beck, Kay Metcalfe, et al.
Pageof 1