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Journal of Pediatric Genetics|September 15, 2016
Cytogenetic analysis in a large series of children with non-syndromic mental retardationInesse Ben Abdallah Bouhjar, Abir Gmidène, Soumaya Mougou-Zrelli, et al.
Scientific Reports|December 20, 2024
Alleviation of drought stress in tomato by foliar application of seafood waste extractImen Ben Sedrine, Sirine Werghi, Afifa Hachef, et al.
Diagnostics (Basel, Switzerland)|August 12, 2023
Morphological and Molecular Characterizations of Cochliomyia hominivorax (Diptera: Calliphoridae) Larvae Responsible for Wound Myiasis in French GuianaMohammad Akhoundi, Alexandre Mathieu, Wajih Hannachi, et al.
La Tunisie Medicale|October 23, 2024
Zohra Chadli, Kmar Kasraoui, Ibtissem Hannachi, et al.
Immunologic Research|July 6, 2024
Association of HLA-G 3'UTR polymorphisms with hepatitis B virus infection in Tunisian populationAhmed Baligh Laaribi, Asma Mehri, Hamza Ben Yahia, et al.
La Tunisie Medicale|December 30, 2006
[Screening and management of coronary artery disease in diabetic patients]Sondos Kraiem, Chedly Abassi, Nizar Annabi, et al.
European Journal of Medical Genetics|June 12, 2012
Chromosomal microarray analysis of functional Xq27-qter disomy and deletion 3p26.3 in a boy with Prader-Willi like features and hypotoniaInesse Ben-Abdallah-Bouhjar, Hanene Hannachi, Audrey Labalme, et al.
International Journal of Pediatric Otorhinolaryngology|July 17, 2013
Compound heterozygosity for dominant and recessive GJB2 mutations in a Tunisian family and association with successful cochlear implant outcomeZied Riahi, Rim Zainine, Yosra Mellouli, et al.
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