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2021-11-19
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Spectrum of Genetic Diseases in Tunisia: Current Situation and Main Milestones Achieved
published
| article-journal
| CC-BY
doi:10.3390/genes12111820
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2022-02-11
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African Genomic Medicine Portal: A Web Portal for Biomedical Applications
published
| article-journal
| CC-BY
doi:10.3390/jpm12020265
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2024-01-03
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Comorbidity of bathing suit ichthyosis and limb-girdle muscular dystrophy type 2 A in a Tunisian patient revealed by Whole Exome Sequencing
published
| article-journal
doi:10.1016/j.gene.2024.148127
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2024-02-26
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Ethnic and functional differentiation of copy number polymorphisms in Tunisian and HapMap population unveils insights on genome organizational plasticity
published
| article-journal
| CC-BY
doi:10.1038/s41598-024-54749-8
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2021-01-08
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A map of copy number variations in the Tunisian population: a valuable tool for medical genomics in North Africa
published
| article-journal
| CC-BY
doi:10.1038/s41525-020-00166-5
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2012-08-21
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Founder mutations in Tunisia: implications for diagnosis in North Africa and Middle East
published
| article-journal
| v1
doi:10.60692/p32z4-7jq79
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2012-08-21
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Founder mutations in Tunisia: implications for diagnosis in North Africa and Middle East
published
| article-journal
| v1
doi:10.60692/dpqf6-ewb51
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2024-02-26
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Ethnic and functional differentiation of copy number polymorphisms in Tunisian and HapMap population unveils insights on genome organizational plasticity
published
| article-journal
| v1
doi:10.60692/325h5-kcp62
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2024-02-26
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Ethnic and functional differentiation of copy number polymorphisms in Tunisian and HapMap population unveils insights on genome organizational plasticity
published
| article-journal
| v1
doi:10.60692/8zscq-rya13
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2021-01-27
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Germline copy number variations in BRCA1/2 negative families: Role in the molecular etiology of hereditary breast cancer in Tunisia
published
| article-journal
| v1
doi:10.60692/f424n-wfq76
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2021-01-27
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Germline copy number variations in BRCA1/2 negative families: Role in the molecular etiology of hereditary breast cancer in Tunisia
published
| article-journal
| v1
doi:10.60692/j691y-xmy90
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2018-12-01
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A genome wide SNP genotyping study in the Tunisian population: specific reporting on a subset of common breast cancer risk loci
published
| article-journal
| v1
doi:10.60692/n796b-ah781
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2019-05-23
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Cytogenetic and molecular diagnosis of Fanconi anemia revealed two hidden phenotypes: Disorder of sex development and cerebro‐oculo‐facio‐skeletal syndrome
published
| article-journal
| v1
doi:10.60692/95ec2-w5x11
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2021-01-08
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A map of copy number variations in the Tunisian population: a valuable tool for medical genomics in North Africa
published
| article-journal
| v1
doi:10.60692/k715d-kbg57
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2019-05-23
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Cytogenetic and molecular diagnosis of Fanconi anemia revealed two hidden phenotypes: Disorder of sex development and cerebro‐oculo‐facio‐skeletal syndrome
published
| article-journal
| v1
doi:10.60692/n2032-wp983
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2015-09-04
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Study of the T16189C variant and mitochondrial lineages in Tunisian and overall Mediterranean region
published
| article-journal
| v1
doi:10.60692/t2yht-kr631
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2015-09-04
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Study of the T16189C variant and mitochondrial lineages in Tunisian and overall Mediterranean region
published
| article-journal
| v1
doi:10.60692/7t83q-73n28
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2024-05-12
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Consanguinité et son impact sur la santé et la dynamique du génome : Un exemple de la Tunisie
published
| article-journal
| CC-BY-NC-ND
doi:10.62438/tunismed.v102i5.4787
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2018-12-01
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A genome wide SNP genotyping study in the Tunisian population: specific reporting on a subset of common breast cancer risk loci
published
| article-journal
| v1
doi:10.60692/53g4k-ssc59
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2021-01-08
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A map of copy number variations in the Tunisian population: a valuable tool for medical genomics in North Africa
published
| article-journal
| v1
doi:10.60692/nkg0j-y1m06
|