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Small 4p16.3 deletions: Three additional patients and review of the literature.
Bernardini L, Radio FC, Acquaviva F, Gorgone C, Postorivo D, Torres B, Alesi V, Magliozzi M, Lonardo F, Monica MD, Nardone AM, Cesario C, Mattina T, Scarano G, Dallapiccola B, Digilio MC, Novelli A. Bernardini L, et al. Among authors: nardone am. Am J Med Genet A. 2018 Nov;176(11):2501-2508. doi: 10.1002/ajmg.a.40512. Epub 2018 Sep 23. Am J Med Genet A. 2018. PMID: 30244530 Review.
Microarray application in prenatal diagnosis: a position statement from the cytogenetics working group of the Italian Society of Human Genetics (SIGU), November 2011.
Novelli A, Grati FR, Ballarati L, Bernardini L, Bizzoco D, Camurri L, Casalone R, Cardarelli L, Cavalli P, Ciccone R, Clementi M, Dalprà L, Gentile M, Gelli G, Grammatico P, Malacarne M, Nardone AM, Pecile V, Simoni G, Zuffardi O, Giardino D. Novelli A, et al. Among authors: nardone am. Ultrasound Obstet Gynecol. 2012 Apr;39(4):384-8. doi: 10.1002/uog.11092. Ultrasound Obstet Gynecol. 2012. PMID: 22262341 Free article. Review.
Another patient with 12q13 microduplication.
Bertoli M, Alesi V, Gullotta F, Zampatti S, Abate MR, Palmieri C, Novelli A, Frontali M, Nardone AM. Bertoli M, et al. Among authors: nardone am. Am J Med Genet A. 2013 Aug;161A(8):2004-8. doi: 10.1002/ajmg.a.35991. Epub 2013 Jul 3. Am J Med Genet A. 2013. PMID: 23824684
Transabdominal coelocentesis as early source of fetal DNA for chromosomal and molecular diagnosis.
Pietropolli A, Vicario R, Peconi C, Zampatti S, Quitadamo MC, Capogna MV, Ragazzo M, Nardone AM, Postorivo D, Spitalieri P, Sarta S, Ratto F, Novelli G, Sangiuolo F, Piccione E, Giardina E. Pietropolli A, et al. Among authors: nardone am. J Matern Fetal Neonatal Med. 2014 Nov;27(16):1656-60. doi: 10.3109/14767058.2013.871697. Epub 2014 Apr 9. J Matern Fetal Neonatal Med. 2014. PMID: 24298912 Clinical Trial.
53 results