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Natural History of Hypertrophic Cardiomyopathy in Noonan Syndrome With Multiple Lentigines.
Monda E, Prosnitz A, Aiello R, Lioncino M, Norrish G, Caiazza M, Drago F, Beattie M, Tartaglia M, Russo MG, Colan SD, Calcagni G, Gelb BD, Kaski JP, Roberts AE, Limongelli G. Monda E, et al. Among authors: prosnitz a. Circ Genom Precis Med. 2023 Aug;16(4):350-358. doi: 10.1161/CIRCGEN.122.003861. Epub 2023 May 18. Circ Genom Precis Med. 2023. PMID: 37199218
Growth in children with congenital heart disease.
Daymont C, Neal A, Prosnitz A, Cohen MS. Daymont C, et al. Among authors: prosnitz a. Pediatrics. 2013 Jan;131(1):e236-42. doi: 10.1542/peds.2012-1157. Epub 2012 Dec 10. Pediatrics. 2013. PMID: 23230071
An atypical deletion of the Williams-Beuren syndrome interval implicates genes associated with defective visuospatial processing and autism.
Edelmann L, Prosnitz A, Pardo S, Bhatt J, Cohen N, Lauriat T, Ouchanov L, González PJ, Manghi ER, Bondy P, Esquivel M, Monge S, Delgado MF, Splendore A, Francke U, Burton BK, McInnes LA. Edelmann L, et al. Among authors: prosnitz a. J Med Genet. 2007 Feb;44(2):136-43. doi: 10.1136/jmg.2006.044537. Epub 2006 Sep 13. J Med Genet. 2007. PMID: 16971481 Free PMC article.