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Page 1
3D-FISH analysis reveals chromatid cohesion defect during interphase in Roberts syndrome.
Dupont C, Bucourt M, Guimiot F, Kraoua L, Smiljkovski D, Le Tessier D, Lebugle C, Gerard B, Spaggiari E, Bourdoncle P, Tabet AC, Benzacken B, Dupont JM. Dupont C, et al. Among authors: kraoua l. Mol Cytogenet. 2014 Sep 30;7(1):59. doi: 10.1186/s13039-014-0059-6. eCollection 2014. Mol Cytogenet. 2014. PMID: 25320640 Free PMC article.
Pseudoaminopterin syndrome.
Kraoua L, Capri Y, Perrin L, Benmansour A, Verloes A. Kraoua L, et al. Am J Med Genet A. 2012 Sep;158A(9):2233-8. doi: 10.1002/ajmg.a.35212. Epub 2012 Jul 18. Am J Med Genet A. 2012. PMID: 22811276
A severe clinical phenotype of Noonan syndrome with neonatal hypertrophic cardiomyopathy in the second case worldwide with RAF1 S259Y neomutation.
Jaouadi H, Chehida AB, Kraoua L, Etchevers HC, Argiro L, Kasdallah N, Blibech S, Delague V, Lévy N, Tebib N, Mrad R, Abdelhak S, Benkhalifa R, Zaffran S. Jaouadi H, et al. Among authors: kraoua l. Genet Res (Camb). 2019 Apr 29;101:e6. doi: 10.1017/S0016672319000041. Genet Res (Camb). 2019. PMID: 31030682 Free PMC article.
Molecular autopsy and clinical family screening in a case of sudden cardiac death reveals ACTN2 mutation related to hypertrophic/dilated cardiomyopathy and a novel LZTR1 variant associated with Noonan syndrome.
Kraoua L, Jaouadi H, Allouche M, Achour A, Kaouther H, Ahmed HB, Chaker L, Maazoul F, Ouarda F, Zaffran S, M'rad R. Kraoua L, et al. Mol Genet Genomic Med. 2022 Jul;10(7):e1954. doi: 10.1002/mgg3.1954. Epub 2022 Jun 3. Mol Genet Genomic Med. 2022. PMID: 35656879 Free PMC article.
Genetic study of Alport syndrome in Tunisia.
Younsi ME, Achour A, Kraoua L, Nesrine M, Sayari T, Abderrahim E, Laabidi J, Zouaghi MK, Kharrat M, Gargah T, Trabelsi M, M'rad R. Younsi ME, et al. Among authors: kraoua l. Pediatr Nephrol. 2025 Jan;40(1):103-116. doi: 10.1007/s00467-024-06474-7. Epub 2024 Aug 14. Pediatr Nephrol. 2025. PMID: 39138691
32 results