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Prenatal Clinical Findings in RASA1-Related Capillary Malformation-Arteriovenous Malformation Syndrome.
Coccia E, Valeri L, Zuntini R, Caraffi SG, Peluso F, Pagliai L, Vezzani A, Pietrangiolillo Z, Leo F, Melli N, Fiorini V, Greco A, Lepri FR, Pisaneschi E, Marozza A, Carli D, Mussa A, Radio FC, Conti B, Iascone M, Gargano G, Novelli A, Tartaglia M, Zuffardi O, Bedeschi MF, Garavelli L. Coccia E, et al. Among authors: tartaglia m. Genes (Basel). 2023 Feb 22;14(3):549. doi: 10.3390/genes14030549. Genes (Basel). 2023. PMID: 36980822 Free PMC article.
Prenatal features of Noonan syndrome: prevalence and prognostic value.
Baldassarre G, Mussa A, Dotta A, Banaudi E, Forzano S, Marinosci A, Rossi C, Tartaglia M, Silengo M, Ferrero GB. Baldassarre G, et al. Among authors: tartaglia m. Prenat Diagn. 2011 Oct;31(10):949-54. doi: 10.1002/pd.2804. Epub 2011 Jul 11. Prenat Diagn. 2011. PMID: 21744363
Hydrops fetalis in a preterm newborn heterozygous for the c.4A>G SHOC2 mutation.
Gargano G, Guidotti I, Balestri E, Vagnarelli F, Rosato S, Comitini G, Wischmeijer A, La Sala GB, Iughetti L, Cordeddu V, Rossi C, Tartaglia M, Garavelli L. Gargano G, et al. Among authors: tartaglia m. Am J Med Genet A. 2014 Apr;164A(4):1015-20. doi: 10.1002/ajmg.a.36376. Epub 2014 Jan 23. Am J Med Genet A. 2014. PMID: 24458587 Free article.
Congenital heart defects in Noonan syndrome and RIT1 mutation.
Calcagni G, Baban A, Lepri FR, Marino B, Tartaglia M, Digilio MC. Calcagni G, et al. Among authors: tartaglia m. Genet Med. 2016 Dec;18(12):1320. doi: 10.1038/gim.2016.137. Epub 2016 Sep 29. Genet Med. 2016. PMID: 27684039 Free article. No abstract available.
893 results