Besma Lakhal

Functional evidence implicating FOXL2 in non-syndromic premature ovarian failure and in the regulation of the transcription factor OSR2

Paul Laissue, Besma Lakhal, Bérénice A. Benayoun et al. · Journal of Medical Genetics · 2009 · 67 citations · Full text

Cytogenetic analyses of premature ovarian failure using karyotyping and interphase fluorescence <i>in situ</i> hybridization (FISH) in a group of 1000 patients

Besma Lakhal, R. Braham, R Berguigua et al. · Clinical Genetics · 2009 · 63 citations

Chromosome Anomalies, Fertility, Cytogenetics +19

NR5A1 (SF-1) gene variants in a group of 26 young women with XX primary ovarian insufficiency

Pascal Philibert, Françoise Paris, Besma Lakhal et al. · Fertility and Sterility · 2012 · 39 citations

Mendelian Disorder, Female Infertility, Genetic Disorder +12

<i><scp>NOBOX</scp></i> is a strong autosomal candidate gene in Tunisian patients with primary ovarian insufficiency

Nouha Bouali, Bruno Francou, Jérôme Bouligand et al. · Clinical Genetics · 2016 · 23 citations

Sequence analysis of the CDKN1B gene in patients with premature ovarian failure reveals a novel mutation potentially related to the phenotype

Diego A. Ojeda, Besma Lakhal, Dora Janneth Fonseca et al. · Fertility and Sterility · 2011 · 21 citations · Full text

Cdkn1b Gene, Female Infertility, Variant Interpretation +11