Rym Meddeb

Identification of Novel BRCA1 Germline Deleterious Variant Among a Tunisian Family

K. Mrad, K. Rahal, S. Hannachi, 2021, Clinical Oncology and Research.

WDR73-related galloway mowat syndrome with collapsing glomerulopathy.

I. Ouertani, R. M’rad, L. Kraoua, 2019, European journal of medical genetics.

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

S. Abdelhak, O. Messaoud, M. B. rekaya, 2020 .

Constitutional mismatch repair deficiency syndrome with atypical features caused by a homozygous MLH1 missense variant (c.1918C>A, p.(Pro640Thr)): a case report

M. Ben Rekaya, S. Rammeh, N. Belguith, 2023, Frontiers in oncology.

Li–Fraumeni syndrome in Tunisian carriers with different and rare tumor phenotype: genotype–phenotype correlation

R. M’rad, S. Hannachi, Hela Sassi, 2022, BMC medical genomics.

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

I. Ouertani, H. Azzouz, L. Kraoua, 2014 .

Exome sequencing and case-control analyses identify RCC1 as a candidate breast cancer susceptibility gene

T. Dörk, R. Geffers, N. Bogdanova, 2018, Geburtshilfe und Frauenheilkunde.