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Hamza Dallali

Showing results (11-20 of 32) with videos related to

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Molecular Genetics & Genomic Medicine|May 25, 2019
Cytogenetic and molecular diagnosis of Fanconi anemia revealed two hidden phenotypes: Disorder of sex development and cerebro-oculo-facio-skeletal syndromeAbir Ben Haj Ali, Ahlem Amouri, Marwa Sayeb, et al.
Frontiers in Genetics|October 25, 2021
Multiallelic Rare Variants in BBS Genes Support an Oligogenic Ciliopathy in a Non-obese Juvenile-Onset Syndromic Diabetic Patient: A Case ReportHamza Dallali, Nadia Kheriji, Wafa Kammoun, et al.
Herz|January 24, 2020
Multiallelic rare variants support an oligogenic origin of sudden cardiac death in the youngHager Jaouadi, Yosra Bouyacoub, Sonia Chabrak, et al.
Plos One|October 20, 2021
Expanding the clinical phenotype associated with NIPAL4 mutation: Study of a Tunisian consanguineous family with erythrokeratodermia variabilis-Like Autosomal Recessive Congenital IchthyosisCherine Charfeddine, Nadia Laroussi, Rahma Mkaouar, et al.
Frontiers in Genetics|January 1, 2024
Whole-exome sequencing reveals novel variants of monogenic diabetes in Tunisia: impact on diagnosis and healthcare managementNadia Kheriji, Hamza Dallali, Ismail Gouiza, et al.
Frontiers in Genetics|January 29, 2024
Expanding the genetic spectrum of mitochondrial diseases in Tunisia: novel variants revealed by whole-exome sequencingIsmail Gouiza, Meriem Hechmi, Abir Zioudi, et al.
Molecular Biology Reports|December 2, 2021
Development of a custom next-generation sequencing panel for the determination of bladder cancer risk in a Tunisian cohortImen Hemissi, Sami Boussetta, Hamza Dallali, et al.
Molecular Biology Reports|January 3, 2022
Correction to: Development of a custom next-generation sequencing panel for the determination of bladder cancer risk in a Tunisian cohortImen Hemissi, Sami Boussetta, Hamza Dallali, et al.
Journal of Human Genetics|January 9, 2020
Identification of a CDH12 potential candidate genetic variant for an autosomal dominant form of transgrediens and progrediens palmoplantar keratoderma in a Tunisian familyCherine Charfeddine, Hamza Dallali, Ghaith Abdessalem, et al.
Diabetes|October 11, 2017
Insights From Molecular Characterization of Adult Patients of Families With Multigenerational DiabetesSerena Pezzilli, Ornella Ludovico, Tommaso Biagini, et al.
Pageof 4

Showing results (11-20 of 32) with videos related to

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Pageof 4
Molecular Genetics & Genomic Medicine|May 25, 2019
Cytogenetic and molecular diagnosis of Fanconi anemia revealed two hidden phenotypes: Disorder of sex development and cerebro-oculo-facio-skeletal syndromeAbir Ben Haj Ali, Ahlem Amouri, Marwa Sayeb, et al.
Frontiers in Genetics|October 25, 2021
Multiallelic Rare Variants in BBS Genes Support an Oligogenic Ciliopathy in a Non-obese Juvenile-Onset Syndromic Diabetic Patient: A Case ReportHamza Dallali, Nadia Kheriji, Wafa Kammoun, et al.
Herz|January 24, 2020
Multiallelic rare variants support an oligogenic origin of sudden cardiac death in the youngHager Jaouadi, Yosra Bouyacoub, Sonia Chabrak, et al.
Plos One|October 20, 2021
Expanding the clinical phenotype associated with NIPAL4 mutation: Study of a Tunisian consanguineous family with erythrokeratodermia variabilis-Like Autosomal Recessive Congenital IchthyosisCherine Charfeddine, Nadia Laroussi, Rahma Mkaouar, et al.
Frontiers in Genetics|January 1, 2024
Whole-exome sequencing reveals novel variants of monogenic diabetes in Tunisia: impact on diagnosis and healthcare managementNadia Kheriji, Hamza Dallali, Ismail Gouiza, et al.
Frontiers in Genetics|January 29, 2024
Expanding the genetic spectrum of mitochondrial diseases in Tunisia: novel variants revealed by whole-exome sequencingIsmail Gouiza, Meriem Hechmi, Abir Zioudi, et al.
Molecular Biology Reports|December 2, 2021
Development of a custom next-generation sequencing panel for the determination of bladder cancer risk in a Tunisian cohortImen Hemissi, Sami Boussetta, Hamza Dallali, et al.
Molecular Biology Reports|January 3, 2022
Correction to: Development of a custom next-generation sequencing panel for the determination of bladder cancer risk in a Tunisian cohortImen Hemissi, Sami Boussetta, Hamza Dallali, et al.
Journal of Human Genetics|January 9, 2020
Identification of a CDH12 potential candidate genetic variant for an autosomal dominant form of transgrediens and progrediens palmoplantar keratoderma in a Tunisian familyCherine Charfeddine, Hamza Dallali, Ghaith Abdessalem, et al.
Diabetes|October 11, 2017
Insights From Molecular Characterization of Adult Patients of Families With Multigenerational DiabetesSerena Pezzilli, Ornella Ludovico, Tommaso Biagini, et al.
Pageof 4