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Cytogenetics and Molecular Investigations detect a Mosaic Variant of Turner Syndrome only Suspected by Non-Invasive Prenatal Testing: Two Case Reports with Negative Ultrasound Examinations.
Libotte F, Carpineto SL, Dello Russo C, Viola A, Margiotti K, Restaldi F, Novelli A, Mesoraca A, Giorlandino C. Libotte F, et al. Among authors: dello russo c. J Med Life. 2020 Oct-Dec;13(4):624-628. doi: 10.25122/jml-2020-0092. J Med Life. 2020. PMID: 33456614 Free PMC article.
Introducing the next generation sequencing in genomic amnio and villuos sampling. The so called "Next Generation Prenatal Diagnosis" (NGPD).
Giorlandino C, Mesoraca A, Bizzoco D, Dello Russo C, Cima A, Di Giacomo G, Cignini P, Padula F, Dugo N, D'Emidio L, Brizzi C, Raffio R, Milite V, Mangiafico L, Coco C, Carcioppolo O, Vigna R, Mastrandrea M, Mobili L. Giorlandino C, et al. Among authors: dello russo c. J Prenat Med. 2014 Jan-Mar;8(1-2):1-10. J Prenat Med. 2014. PMID: 25332753 Free PMC article. No abstract available.
Agnathia-Otocephaly Complex Due to a De Novo Deletion in the OTX2 Gene.
Fabiani M, Libotte F, Margiotti K, Tannous DKI, Sparacino D, D'Aleo MP, Monaco F, Dello Russo C, Mesoraca A, Giorlandino C. Fabiani M, et al. Among authors: dello russo c. Genes (Basel). 2022 Dec 2;13(12):2269. doi: 10.3390/genes13122269. Genes (Basel). 2022. PMID: 36553536 Free PMC article.
98 results