Author:
Molck Miriam Coelho,Simioni Milena,Paiva Vieira Társis,Sgardioli Ilária Cristina,Paoli Monteiro Fabíola,Souza Josiane,Fett-Conte Agnes Cristina,Félix Têmis Maria,Lopes Monlléo Isabella,Gil-da-Silva-Lopes Vera Lúcia
Subject
Pediatrics, Perinatology, and Child Health
Reference32 articles.
1. Genetics of congenital heart disease: the glass half empty;Fahed;Circ Res.,2013
2. The Philadelphia story: the 22q11.2 deletion: report on 250 patients;McDonald-McGinn;Genet Couns.,1999
3. Copy-number variation of the glucose transporter gene SLC2A3 and congenital heart defects in the 22q11.2 deletion syndrome;Mlynarski;Am J Hum Genet.,2015
4. Chromosome 22q11.2 microdeletion in children with conotruncal heart defects: frequency, associated cardiovascular anomalies, and outcome following cardiac surgery;Ziolkowska;Eur J Pediatr.,2008
5. 8p23.1 Interstitial deletion in a patient with congenital cardiopathy, neurobehavioral disorders, and minor signs suggesting 22q11.2 deletion syndrome;Molck;J Dev Behav Pediatr.,2015
Cited by
28 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献