khouloud Rjiba

Clinical and molecular characterization of 1q43q44 deletion and corpus callosum malformations: 2 new cases and literature review

A. Saâd, N. Gouider-Khouja, S. Dimassi, 2022, Molecular Cytogenetics.

Disorders of sex development in Wolf–Hirschhorn syndrome: a genotype–phenotype correlation and MSX1 as candidate gene

A. Saâd, S. Mougou-Zerelli, W. Slimani, 2021, Molecular Cytogenetics.

Additional evidence for the role of chromosomal imbalances and SOX8, ZNRF3 and HHAT gene variants in early human testis development

M. Gribaa, K. McElreavey, A. Saâd, 2023, Reproductive Biology and Endocrinology.

Response to growth hormone therapy in ring chromosome 15: Review and evidence from a new case on possible beneficial effect in neurodevelopment.

H. Bouzidi, A. Saad, S. Mougou, 2023, Growth hormone & IGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society.

Further report of MEDS syndrome: Clinical and molecular delineation of a new Tunisian case.

K. McElreavey, A. Saâd, S. Mougou-Zerelli, 2021, European journal of medical genetics.

ORI GI NAL AR TIC LE

K. McElreavey, A. Saâd, S. Mougou-Zerelli, 2023 .