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A new era of genetic testing in congenital heart disease: A review.
Morrish AM, Smith J, Enriquez A, Sholler GF, Mervis J, Dunwoodie SL, Kirk EP, Winlaw DS, Blue GM. Morrish AM, et al. Among authors: winlaw ds. Trends Cardiovasc Med. 2022 Jul;32(5):311-319. doi: 10.1016/j.tcm.2021.04.011. Epub 2021 May 5. Trends Cardiovasc Med. 2022. PMID: 33964404 Review.
Outcomes following surgery for congenital heart disease in low-birthweight infants.
Dimmick S, Walker K, Badawi N, Halliday R, Cooper SG, Nicholson IA, Sherwood M, Chard RB, Hawker R, Lau KC, Jones O, Grant PW, Sholler GF, Winlaw DS; Neonatal Intensive Care Units Study (NICUS) of the New South Wales Pregnancy and Newborn Services Network. Dimmick S, et al. Among authors: winlaw ds. J Paediatr Child Health. 2007 May;43(5):370-5. doi: 10.1111/j.1440-1754.2007.01082.x. J Paediatr Child Health. 2007. PMID: 17489827
Mutations in cardiac T-box factor gene TBX20 are associated with diverse cardiac pathologies, including defects of septation and valvulogenesis and cardiomyopathy.
Kirk EP, Sunde M, Costa MW, Rankin SA, Wolstein O, Castro ML, Butler TL, Hyun C, Guo G, Otway R, Mackay JP, Waddell LB, Cole AD, Hayward C, Keogh A, Macdonald P, Griffiths L, Fatkin D, Sholler GF, Zorn AM, Feneley MP, Winlaw DS, Harvey RP. Kirk EP, et al. Among authors: winlaw ds. Am J Hum Genet. 2007 Aug;81(2):280-91. doi: 10.1086/519530. Epub 2007 Jun 15. Am J Hum Genet. 2007. PMID: 17668378 Free PMC article.
GATA4 mutations in 357 unrelated patients with congenital heart malformation.
Butler TL, Esposito G, Blue GM, Cole AD, Costa MW, Waddell LB, Walizada G, Sholler GF, Kirk EP, Feneley M, Harvey RP, Winlaw DS. Butler TL, et al. Among authors: winlaw ds. Genet Test Mol Biomarkers. 2010 Dec;14(6):797-802. doi: 10.1089/gtmb.2010.0028. Epub 2010 Sep 27. Genet Test Mol Biomarkers. 2010. PMID: 20874241
227 results