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Plos One
|
April 14, 2018
Pharmacogenetic landscape of Metabolic Syndrome components drug response in Tunisia and comparison with worldwide populations
Haifa Jmel, Lilia Romdhane, Yosra Ben Halima, et al.
Plos One
|
January 27, 2021
Germline copy number variations in BRCA1/2 negative families: Role in the molecular etiology of hereditary breast cancer in Tunisia
Maroua Boujemaa, Yosr Hamdi, Nesrine Mejri, et al.
Journal of Translational Medicine
|
June 29, 2019
Identification of novel pathogenic MSH2 mutation and new DNA repair genes variants: investigation of a Tunisian Lynch syndrome family with discordant twins
Amira Jaballah-Gabteni, Haifa Tounsi, Maria Kabbage, et al.
Bioscience Reports
|
September 12, 2022
Next-generation sequencing of Tunisian Leigh syndrome patients reveals novel variations: impact for diagnosis and treatment
Meriem Hechmi, Majida Charif, Ichraf Kraoua, et al.
Journal of Dermatological Science
|
November 25, 2017
Whole Exome Sequencing allows the identification of two novel groups of Xeroderma pigmentosum in Tunisia, XP-D and XP-E: Impact on molecular diagnosis
Mariem Ben Rekaya, Chokri Naouali, Olfa Messaoud, et al.
Acta Diabetologica
|
January 19, 2019
Genetic characterization of suspected MODY patients in Tunisia by targeted next-generation sequencing
Hamza Dallali, Serena Pezzilli, Meriem Hechmi, et al.
Annales D'Endocrinologie
|
June 19, 2017
Association of apolipoprotein A5 gene variants with metabolic syndrome in Tunisian population
Rym Kefi, Meriem Hechmi, Hamza Dallali, et al.
Plos One
|
October 6, 2021
Alpha-mannosidosis in Tunisian consanguineous families: Potential involvement of variants in GHR and SLC19A3 genes in the variable expressivity of cognitive impairment
Rahma Mkaouar, Zied Riahi, Cherine Charfeddine, et al.
Biomed Research International
|
October 19, 2023
PHINDaccess Hackathons for COVID-19 and Host-Pathogen Interaction: Lessons Learned and Recommendations for Low- and Middle-Income Countries
Kais Ghedira, Hamza Dallali, Monia Ardhaoui, et al.
Frontiers in Genetics
|
May 7, 2024
Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health
Rahma Mkaouar, Zied Riahi, Jihene Marrakchi, et al.
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Showing results (21-30 of 32) with videos related to
Sort By:
Page
of 4
Plos One
|
April 14, 2018
Pharmacogenetic landscape of Metabolic Syndrome components drug response in Tunisia and comparison with worldwide populations
Haifa Jmel, Lilia Romdhane, Yosra Ben Halima, et al.
Plos One
|
January 27, 2021
Germline copy number variations in BRCA1/2 negative families: Role in the molecular etiology of hereditary breast cancer in Tunisia
Maroua Boujemaa, Yosr Hamdi, Nesrine Mejri, et al.
Journal of Translational Medicine
|
June 29, 2019
Identification of novel pathogenic MSH2 mutation and new DNA repair genes variants: investigation of a Tunisian Lynch syndrome family with discordant twins
Amira Jaballah-Gabteni, Haifa Tounsi, Maria Kabbage, et al.
Bioscience Reports
|
September 12, 2022
Next-generation sequencing of Tunisian Leigh syndrome patients reveals novel variations: impact for diagnosis and treatment
Meriem Hechmi, Majida Charif, Ichraf Kraoua, et al.
Journal of Dermatological Science
|
November 25, 2017
Whole Exome Sequencing allows the identification of two novel groups of Xeroderma pigmentosum in Tunisia, XP-D and XP-E: Impact on molecular diagnosis
Mariem Ben Rekaya, Chokri Naouali, Olfa Messaoud, et al.
Acta Diabetologica
|
January 19, 2019
Genetic characterization of suspected MODY patients in Tunisia by targeted next-generation sequencing
Hamza Dallali, Serena Pezzilli, Meriem Hechmi, et al.
Annales D'Endocrinologie
|
June 19, 2017
Association of apolipoprotein A5 gene variants with metabolic syndrome in Tunisian population
Rym Kefi, Meriem Hechmi, Hamza Dallali, et al.
Plos One
|
October 6, 2021
Alpha-mannosidosis in Tunisian consanguineous families: Potential involvement of variants in GHR and SLC19A3 genes in the variable expressivity of cognitive impairment
Rahma Mkaouar, Zied Riahi, Cherine Charfeddine, et al.
Biomed Research International
|
October 19, 2023
PHINDaccess Hackathons for COVID-19 and Host-Pathogen Interaction: Lessons Learned and Recommendations for Low- and Middle-Income Countries
Kais Ghedira, Hamza Dallali, Monia Ardhaoui, et al.
Frontiers in Genetics
|
May 7, 2024
Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health
Rahma Mkaouar, Zied Riahi, Jihene Marrakchi, et al.
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of 4