Yıl: 2022 Cilt: 26 Sayı: 2 Sayfa Aralığı: 149 - 150 Metin Dili: İngilizce DOI: 10.5152/AnatolJCardiol.2021.554 İndeks Tarihi: 17-06-2022

A rare etiology of tetralogy of Fallot with pulmonary atresia: Renpenning syndrome

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  • 1. Liu Y, Chen S, Zühlke L, Black GC, Choy MK, Li N, et al. Global birth prevalence of congenital heart defects 1970-2017: updated systematic review and meta-analysis of 260 studies. Int J Epidemiol 2019; 48: 455-63. [Crossref]
  • 2. Blue GM, Kirk EP, Giannoulatou E, Sholler GF, Dunwoodie SL, Harvey RP, et al. Advances in the Genetics of Congenital Heart Disease: A Clinician’s Guide. J Am Coll Cardiol 2017; 69: 859-70. [Crossref]
  • 3. Peng R, Zheng J, Xie HN, He M, Lin MF. Genetic anomalies in fetuses with tetralogy of Fallot by using high-definition chromosomal microarray analysis. Cardiovasc Ultrasound 2019; 17: 8. [Crossref]
  • 4. Morgenthau A, Frishman WH. Genetic Origins of Tetralogy of Fallot. Cardiol Rev 2018; 26: 86-92. [Crossref]
  • 5. Apitz C, Webb GD, Redington AN. Tetralogy of Fallot. Lancet 2009; 374: 1462-71. [Crossref]
  • 6. Stevenson RE, Bennett CW, Abidi F, Kleefstra T, Porteous M, Simensen RJ, et al. Renpenning syndrome comes into focus. Am J Med Genet A 2005; 134: 415-21. [Crossref]
  • 7. Germanaud D, Rossi M, Bussy G, Gérard D, Hertz-Pannier L, Blanchet P, et al. The Renpenning syndrome spectrum: new clinical insights supported by 13 new PQBP1-mutated males. Clin Genet 2011; 79: 225-35. [Crossref]
  • 8. Miller DT, Adam MP, Aradhya S, Biesecker LG, Brothman AR, Carter NP, et al. Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies. Am J Hum Genet 2010; 86: 749-64. [Crossref]
  • 9. Liu X, Dou LX, Han J, Zhang ZC. The Renpenning syndrome-associated protein PQBP1 facilitates the nuclear import of splicing factor TXNL4A through the karyopherin β2 receptor. J Biol Chem 2020; 295: 4093-100. [Crossref]
APA Kaymakcalan H, Ercan-Sencicek A, Cebeci A, Dong W (2022). A rare etiology of tetralogy of Fallot with pulmonary atresia: Renpenning syndrome. , 149 - 150. 10.5152/AnatolJCardiol.2021.554
Chicago Kaymakcalan Hande,Ercan-Sencicek Adife,Cebeci Ayse Nurcan,Dong Weilai A rare etiology of tetralogy of Fallot with pulmonary atresia: Renpenning syndrome. (2022): 149 - 150. 10.5152/AnatolJCardiol.2021.554
MLA Kaymakcalan Hande,Ercan-Sencicek Adife,Cebeci Ayse Nurcan,Dong Weilai A rare etiology of tetralogy of Fallot with pulmonary atresia: Renpenning syndrome. , 2022, ss.149 - 150. 10.5152/AnatolJCardiol.2021.554
AMA Kaymakcalan H,Ercan-Sencicek A,Cebeci A,Dong W A rare etiology of tetralogy of Fallot with pulmonary atresia: Renpenning syndrome. . 2022; 149 - 150. 10.5152/AnatolJCardiol.2021.554
Vancouver Kaymakcalan H,Ercan-Sencicek A,Cebeci A,Dong W A rare etiology of tetralogy of Fallot with pulmonary atresia: Renpenning syndrome. . 2022; 149 - 150. 10.5152/AnatolJCardiol.2021.554
IEEE Kaymakcalan H,Ercan-Sencicek A,Cebeci A,Dong W "A rare etiology of tetralogy of Fallot with pulmonary atresia: Renpenning syndrome." , ss.149 - 150, 2022. 10.5152/AnatolJCardiol.2021.554
ISNAD Kaymakcalan, Hande vd. "A rare etiology of tetralogy of Fallot with pulmonary atresia: Renpenning syndrome". (2022), 149-150. https://doi.org/10.5152/AnatolJCardiol.2021.554
APA Kaymakcalan H, Ercan-Sencicek A, Cebeci A, Dong W (2022). A rare etiology of tetralogy of Fallot with pulmonary atresia: Renpenning syndrome. The Anatolian Journal of Cardiology, 26(2), 149 - 150. 10.5152/AnatolJCardiol.2021.554
Chicago Kaymakcalan Hande,Ercan-Sencicek Adife,Cebeci Ayse Nurcan,Dong Weilai A rare etiology of tetralogy of Fallot with pulmonary atresia: Renpenning syndrome. The Anatolian Journal of Cardiology 26, no.2 (2022): 149 - 150. 10.5152/AnatolJCardiol.2021.554
MLA Kaymakcalan Hande,Ercan-Sencicek Adife,Cebeci Ayse Nurcan,Dong Weilai A rare etiology of tetralogy of Fallot with pulmonary atresia: Renpenning syndrome. The Anatolian Journal of Cardiology, vol.26, no.2, 2022, ss.149 - 150. 10.5152/AnatolJCardiol.2021.554
AMA Kaymakcalan H,Ercan-Sencicek A,Cebeci A,Dong W A rare etiology of tetralogy of Fallot with pulmonary atresia: Renpenning syndrome. The Anatolian Journal of Cardiology. 2022; 26(2): 149 - 150. 10.5152/AnatolJCardiol.2021.554
Vancouver Kaymakcalan H,Ercan-Sencicek A,Cebeci A,Dong W A rare etiology of tetralogy of Fallot with pulmonary atresia: Renpenning syndrome. The Anatolian Journal of Cardiology. 2022; 26(2): 149 - 150. 10.5152/AnatolJCardiol.2021.554
IEEE Kaymakcalan H,Ercan-Sencicek A,Cebeci A,Dong W "A rare etiology of tetralogy of Fallot with pulmonary atresia: Renpenning syndrome." The Anatolian Journal of Cardiology, 26, ss.149 - 150, 2022. 10.5152/AnatolJCardiol.2021.554
ISNAD Kaymakcalan, Hande vd. "A rare etiology of tetralogy of Fallot with pulmonary atresia: Renpenning syndrome". The Anatolian Journal of Cardiology 26/2 (2022), 149-150. https://doi.org/10.5152/AnatolJCardiol.2021.554