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MED12 Mutation in Two Families with X-Linked Ohdo Syndrome.
Rocchetti L, Evangelista E, De Falco L, Savarese G, Savarese P, Ruggiero R, D'Amore L, Sensi A, Fico A. Rocchetti L, et al. Among authors: de falco l. Genes (Basel). 2021 Aug 27;12(9):1328. doi: 10.3390/genes12091328. Genes (Basel). 2021. PMID: 34573309 Free PMC article.
A Case Report of a Feto-Placental Mosaicism Involving a Segmental Aneuploidy: A Challenge for Genome Wide Screening by Non-Invasive Prenatal Testing of Cell-Free DNA in Maternal Plasma.
De Falco L, Vitiello G, Savarese G, Suero T, Ruggiero R, Savarese P, Ianniello M, Petrillo N, Bruno M, Legnante A, Passaretti FF, Ardisia C, Di Spiezio Sardo A, Fico A. De Falco L, et al. Genes (Basel). 2023 Mar 7;14(3):668. doi: 10.3390/genes14030668. Genes (Basel). 2023. PMID: 36980940 Free PMC article.
[New types of microcytic anemia].
Iolascon A, De Falco L, Boschetto L, Piscopo C, Pirolo C, Di Noce F. Iolascon A, et al. Among authors: de falco l. Minerva Pediatr. 2007 Oct;59(5):525-7. Minerva Pediatr. 2007. PMID: 17947902 Italian. No abstract available.
Congenital dyserythropoietic anaemias: new acquisitions.
Iolascon A, Russo R, Esposito MR, Piscopo C, Asci R, De Falco L, Di Noce F. Iolascon A, et al. Among authors: de falco l. Blood Transfus. 2011 Jul;9(3):278-80. doi: 10.2450/2010.0085-10. Epub 2010 Dec 13. Blood Transfus. 2011. PMID: 21251457 Free PMC article. Review. No abstract available.
63 results