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Clinical and molecular study of DiGeorge sequence.
Levy-Mozziconacci A, Wernert F, Scambler P, Rouault F, Metras D, Kreitman B, Depetris D, Mattei MG, Philip N. Levy-Mozziconacci A, et al. Eur J Pediatr. 1994 Nov;153(11):813-20. doi: 10.1007/BF01972889. Eur J Pediatr. 1994. PMID: 7843195
Prenatal diagnosis of 22q11 microdeletion.
Levy-Mozziconacci A, Piquet C, Heurtevin PC, Philip N. Levy-Mozziconacci A, et al. Prenat Diagn. 1997 Nov;17(11):1033-7. Prenat Diagn. 1997. PMID: 9399351 Clinical Trial.
Molecular background of D-negative phenotype in the Tunisian population.
Moussa H, Tsochandaridis M, Chakroun T, Jridi S, Abdelneji B, Hmida S, Silvy M, Bailly P, Gabert J, Levy-Mozziconacci A, Jemni-Yacoub S. Moussa H, et al. Transfus Med. 2012 Jun;22(3):192-8. doi: 10.1111/j.1365-3148.2012.01142.x. Epub 2012 Mar 16. Transfus Med. 2012. PMID: 22420413
20 results