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Rym Meddeb

Tunis University

7

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15

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Identification of Novel BRCA1 Germline Deleterious Variant Among a Tunisian Family

2021 Computers & Operations Research
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Whole exome sequencing reveals a combination of rare high and low penetrance variants that correlates with familial breast cancer relative risk

2020
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WDR73-related galloway mowat syndrome with collapsing glomerulopathy

2018 European Journal of Medical Genetics
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Exome sequencing and case-control analyses identify RCC1 as a candidate breast cancer susceptibility gene

2018
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Clinical and Molecular Cytogenetic Study of 38 Williams-Beuren Syndrome Tunisian Patients

2014 Open Journal of Genetics
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