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Gene|September 7, 2012
Mutational screening of SF1 and WNT4 in Tunisian women with premature ovarian failureBesma Lakhal, Sonia Ben-Hadj-Khalifa, Nouha Bouali, et al.
Fertility and Sterility|November 17, 2012
NR5A1 (SF-1) gene variants in a group of 26 young women with XX primary ovarian insufficiencyPascal Philibert, Françoise Paris, Besma Lakhal, et al.
Reproductive Biomedicine Online|January 31, 2012
Screening for mutations of the FOXO4 gene in premature ovarian failure patientsDora Janeth Fonseca, Eliana Garzón, Besma Lakhal, et al.
Fertility and Sterility|May 18, 2011
Sequence analysis of the CDKN1B gene in patients with premature ovarian failure reveals a novel mutation potentially related to the phenotypeDiego Ojeda, Besma Lakhal, Dora Janneth Fonseca, et al.
Annales D'Endocrinologie|November 24, 2015
Analysis of FMR1 gene premutation and X chromosome cytogenetic abnormalities in 100 Tunisian patients presenting premature ovarian failureNouha Bouali, Dorra Hmida, Soumaya Mougou, et al.
Translational Research : the Journal of Laboratory and Clinical Medicine|June 20, 2012
CITED2 mutations potentially cause idiopathic premature ovarian failureDora Janeth Fonseca, Diego Ojeda, Besma Lakhal, et al.
Open Biology|November 3, 2016
Association of FOXD1 variants with adverse pregnancy outcomes in mice and humansPaul Laissue, Besma Lakhal, Magalie Vatin, et al.
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