Cardiac function in adolescents and young adults with 22q11.2 deletion syndrome without congenital heart disease-Reference-Cited by-同舟云学术

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Cardiac function in adolescents and young adults with 22q11.2 deletion syndrome without congenital heart disease

Published:2023-01 Issue:1 Volume:66 Page:104651
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Putotto Carolina^ORCID,Unolt Marta,Lambiase Caterina,Marchetti Flaminia,Anaclerio Silvia,Favoriti Alessandra,Tancredi Giancarlo,Mastromoro Gioia^ORCID,Pugnaloni Flaminia^ORCID,Liberati Natascia,De Luca Enrica,Tarani Luigi,De Canditiis Daniela^ORCID,Caputo Viviana,Bernardini Laura,Digilio Maria Cristina,Marino Bruno^ORCID,Versacci Paolo^ORCID

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics,General Medicine

Reference53 articles.

1. Left ventricular systolic dysfunction in asymptomatic Marfan syndrome patients is related to the severity of gene mutation: insights from the novel three dimensional speckle tracking echocardiography;Abd El Rahman;PLoS One,2015

2. Tbx1: transcriptional and developmental functions;Baldini;Curr. Top. Dev. Biol.,2017

3. Assessment of cardiac function in absence of congenital and acquired heart disease in patients with Down syndrome;Balli;World J Pediatr,2016

4. Premature death in adults with 22q11.2 deletion syndrome;Bassett;J. Med. Genet.,2009

5. 22q11.21 deletion syndromes: a review of proximal, central, and distal deletions and their associated features;Burnside;Cytogenet. Genome Res.,2015

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