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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
Effectiveness and costs of non-invasive foetal RHD genotyping in rhesus-D negative mothers: a French multicentric two-arm study of 850 women.
Darlington M, Carbonne B, Mailloux A, Brossard Y, Levy-Mozziconacci A, Cortey A, Maoulida H, Simon T, Rousseau A, Durand-Zaleski I; GENIFERH1 Study Group. Darlington M, et al. Among authors: levy mozziconacci a. BMC Pregnancy Childbirth. 2018 Dec 14;18(1):496. doi: 10.1186/s12884-018-2114-5. BMC Pregnancy Childbirth. 2018. PMID: 30547830 Free PMC article. Clinical Trial.
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.
20 results