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

Nessrine Mezzi

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

Pageof 1
Sort By:
La Tunisie Medicale|May 27, 2024
Nessrine Mezzi, Najla Abassi, Faten Fatnassi, et al.
Annual Review of Genomics and Human Genetics|May 1, 2019
Consanguinity and Inbreeding in Health and Disease in North African PopulationsLilia Romdhane, Nessrine Mezzi, Yosr Hamdi, et al.
NPJ Genomic Medicine|January 9, 2021
A map of copy number variations in the Tunisian population: a valuable tool for medical genomics in North AfricaLilia Romdhane, Nessrine Mezzi, Hamza Dallali, et al.
Gene|January 5, 2024
Comorbidity of bathing suit ichthyosis and limb-girdle muscular dystrophy type 2 A in a Tunisian patient revealed by Whole Exome SequencingNessrine Mezzi, Anissa Zaouak, Rahma Mkaouar, et al.
Scientific Reports|February 27, 2024
Ethnic and functional differentiation of copy number polymorphisms in Tunisian and HapMap population unveils insights on genome organizational plasticityLilia Romdhane, Sameh Kefi, Nessrine Mezzi, et al.
Genes|November 27, 2021
Spectrum of Genetic Diseases in Tunisia: Current Situation and Main Milestones AchievedNessrine Mezzi, Olfa Messaoud, Rahma Mkaouar, et al.
Frontiers in Pharmacology|June 4, 2026
Pharmacogenomics of treatment toxicities in pediatric B-Cell ALL: toward safer precision therapyMeriem Lameri, Tarek Kamergi, Ameni Brahim, et al.
Frontiers in Genetics|May 7, 2024
Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory healthRahma Mkaouar, Zied Riahi, Jihene Marrakchi, et al.
Frontiers in Genetics|July 10, 2024
Corrigendum: Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory healthRahma Mkaouar, Zied Riahi, Jihene Marrakchi, et al.
Journal of Personalized Medicine|February 25, 2022
African Genomic Medicine Portal: A Web Portal for Biomedical ApplicationsHoucemeddine Othman, Lyndon Zass, Jorge E B da Rocha, et al.
Pageof 1

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

Sort By:
Pageof 1
La Tunisie Medicale|May 27, 2024
Nessrine Mezzi, Najla Abassi, Faten Fatnassi, et al.
Annual Review of Genomics and Human Genetics|May 1, 2019
Consanguinity and Inbreeding in Health and Disease in North African PopulationsLilia Romdhane, Nessrine Mezzi, Yosr Hamdi, et al.
NPJ Genomic Medicine|January 9, 2021
A map of copy number variations in the Tunisian population: a valuable tool for medical genomics in North AfricaLilia Romdhane, Nessrine Mezzi, Hamza Dallali, et al.
Gene|January 5, 2024
Comorbidity of bathing suit ichthyosis and limb-girdle muscular dystrophy type 2 A in a Tunisian patient revealed by Whole Exome SequencingNessrine Mezzi, Anissa Zaouak, Rahma Mkaouar, et al.
Scientific Reports|February 27, 2024
Ethnic and functional differentiation of copy number polymorphisms in Tunisian and HapMap population unveils insights on genome organizational plasticityLilia Romdhane, Sameh Kefi, Nessrine Mezzi, et al.
Genes|November 27, 2021
Spectrum of Genetic Diseases in Tunisia: Current Situation and Main Milestones AchievedNessrine Mezzi, Olfa Messaoud, Rahma Mkaouar, et al.
Frontiers in Pharmacology|June 4, 2026
Pharmacogenomics of treatment toxicities in pediatric B-Cell ALL: toward safer precision therapyMeriem Lameri, Tarek Kamergi, Ameni Brahim, et al.
Frontiers in Genetics|May 7, 2024
Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory healthRahma Mkaouar, Zied Riahi, Jihene Marrakchi, et al.
Frontiers in Genetics|July 10, 2024
Corrigendum: Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory healthRahma Mkaouar, Zied Riahi, Jihene Marrakchi, et al.
Journal of Personalized Medicine|February 25, 2022
African Genomic Medicine Portal: A Web Portal for Biomedical ApplicationsHoucemeddine Othman, Lyndon Zass, Jorge E B da Rocha, et al.
Pageof 1