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Anomalies in Human Sex Determination: Usefulness of a Combined Cytogenetic Approach to Characterize an Additional Case with Xp Functional Disomy Associated with 46,XY Gonadal Dysgenesis.
Rjiba K, Slimani W, Gaddas M, Hassine IH, Jelloul A, Khelifa HB, El Amri F, Zaouali M, Mcelreavey K, Saad A, Mougou-Zerelli S. Rjiba K, et al. J Clin Res Pediatr Endocrinol. 2023 Feb 27;15(1):25-34. doi: 10.4274/jcrpe.galenos.2022.2022-3-15. Epub 2022 Aug 19. J Clin Res Pediatr Endocrinol. 2023. PMID: 35984215 Free PMC article.
Additional evidence for the role of chromosomal imbalances and SOX8, ZNRF3 and HHAT gene variants in early human testis development.
Rjiba K, Mougou-Zerelli S, Hamida IH, Saad G, Khadija B, Jelloul A, Slimani W, Hasni Y, Dimassi S, Khelifa HB, Sallem A, Kammoun M, Abdallah HH, Gribaa M, Bignon-Topalovic J, Chelly S, Khairi H, Bibi M, Kacem M, Saad A, Bashamboo A, McElreavey K. Rjiba K, et al. Reprod Biol Endocrinol. 2023 Jan 11;21(1):2. doi: 10.1186/s12958-022-01045-7. Reprod Biol Endocrinol. 2023. PMID: 36631813 Free PMC article.
[No title available]
[No authors listed] [No authors listed] PMID: 36876341
Bloom syndrome in children: unusual case of early onset lung damage.
Ajmi H, Trabelsi I, Rjiba K, Mabrouk S, Zouari N, Mougou-Zerelli S, Verloes A, Abroug S. Ajmi H, et al. Among authors: rjiba k. Clin Dysmorphol. 2023 Apr 1;32(2):95-96. doi: 10.1097/MCD.0000000000000448. Epub 2023 Feb 17. Clin Dysmorphol. 2023. PMID: 36876347 No abstract available.
14 results