Xing J, Wang H, Xie Y, Fan T, Cui C, Li Y
Open Life Sci. 2023; 18(1):20220593.
PMID: 37215497
PMC: 10199322.
DOI: 10.1515/biol-2022-0593.
Putotto C, Pugnaloni F, Unolt M, Maiolo S, Trezzi M, Digilio M
Children (Basel). 2022; 9(6).
PMID: 35740709
PMC: 9222179.
DOI: 10.3390/children9060772.
Peng J, Wang Q, Meng Z, Wang J, Zhou Y, Zhou S
FEBS Open Bio. 2020; 11(2):375-385.
PMID: 33211401
PMC: 7876499.
DOI: 10.1002/2211-5463.13044.
Traisrisilp K, Tongprasert F, Srisupundit K, Luewan S, Tongsong T
Obstet Gynecol Sci. 2020; 63(3):330-336.
PMID: 32489978
PMC: 7231935.
DOI: 10.5468/ogs.2020.63.3.330.
Shi X, Zhang L, Bai K, Xie H, Shi T, Zhang R
Comput Struct Biotechnol J. 2020; 18:381-392.
PMID: 32128068
PMC: 7044470.
DOI: 10.1016/j.csbj.2020.01.011.
Identification of Rare Copy Number Variants Associated With Pulmonary Atresia With Ventricular Septal Defect.
Xie H, Hong N, Zhang E, Li F, Sun K, Yu Y
Front Genet. 2019; 10:15.
PMID: 30745907
PMC: 6360179.
DOI: 10.3389/fgene.2019.00015.
Congenital heart diseases and cardiovascular abnormalities in 22q11.2 deletion syndrome: From well-established knowledge to new frontiers.
Unolt M, Versacci P, Anaclerio S, Lambiase C, Calcagni G, Trezzi M
Am J Med Genet A. 2018; 176(10):2087-2098.
PMID: 29663641
PMC: 6497171.
DOI: 10.1002/ajmg.a.38662.
Ductal stent implantation in tetralogy of fallot with aortic arch abnormality.
Tola H, Ergul Y, Saygi M, Ozyilmaz I, Guzeltas A, Odemis E
Tex Heart Inst J. 2015; 42(3):281-4.
PMID: 26175649
PMC: 4473630.
DOI: 10.14503/THIJ-13-3373.
Rare de novo copy number variants in patients with congenital pulmonary atresia.
Xie L, Chen J, Zhang W, Wang S, Zhao T, Huang C
PLoS One. 2014; 9(5):e96471.
PMID: 24826987
PMC: 4020819.
DOI: 10.1371/journal.pone.0096471.
A variant in the carboxyl-terminus of connexin 40 alters GAP junctions and increases risk for tetralogy of Fallot.
Guida V, Ferese R, Rocchetti M, Bonetti M, Sarkozy A, Cecchetti S
Eur J Hum Genet. 2012; 21(1):69-75.
PMID: 22713807
PMC: 3533258.
DOI: 10.1038/ejhg.2012.109.
Clinical manifestations of Deletion 22q11.2 syndrome (DiGeorge/Velo-Cardio-Facial syndrome).
Digilio M, Marino B, Capolino R, Dallapiccola B
Images Paediatr Cardiol. 2012; 7(2):23-34.
PMID: 22368650
PMC: 3232571.
Extracardiac features predicting 22q11.2 deletion syndrome in adult congenital heart disease.
Fung W, Chow E, Webb G, Gatzoulis M, Bassett A
Int J Cardiol. 2008; 131(1):51-8.
PMID: 18191243
PMC: 3139626.
DOI: 10.1016/j.ijcard.2007.08.141.
Laterality of the aortic arch and anomalies of the subclavian artery-reliable indicators for 22q11.2 deletion syndromes?.
Rauch R, Rauch A, Koch A, Zink S, Kaulitz R, Girisch M
Eur J Pediatr. 2004; 163(11):642-5.
PMID: 15300432
DOI: 10.1007/s00431-004-1518-6.
Monosomy 22q11 in patients with pulmonary atresia, ventricular septal defect, and major aortopulmonary collateral arteries.
Hofbeck M, Rauch A, Buheitel G, Leipold G, Von Der Emde J, Pfeiffer R
Heart. 1998; 79(2):180-5.
PMID: 9538313
PMC: 1728610.
DOI: 10.1136/hrt.79.2.180.
Recurrence risk figures for isolated tetralogy of Fallot after screening for 22q11 microdeletion.
Digilio M, Marino B, Giannotti A, Toscano A, Dallapiccola B
J Med Genet. 1997; 34(3):188-90.
PMID: 9132487
PMC: 1050890.
DOI: 10.1136/jmg.34.3.188.