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The genetic architecture of pediatric cardiomyopathy.
Ware SM, Bhatnagar S, Dexheimer PJ, Wilkinson JD, Sridhar A, Fan X, Shen Y, Tariq M, Schubert JA, Colan SD, Shi L, Canter CE, Hsu DT, Bansal N, Webber SA, Everitt MD, Kantor PF, Rossano JW, Pahl E, Rusconi P, Lee TM, Towbin JA, Lal AK, Chung WK, Miller EM, Aronow B, Martin LJ, Lipshultz SE; Pediatric Cardiomyopathy Registry Study Group. Ware SM, et al. Among authors: towbin ja. Am J Hum Genet. 2022 Feb 3;109(2):282-298. doi: 10.1016/j.ajhg.2021.12.006. Epub 2022 Jan 12. Am J Hum Genet. 2022. PMID: 35026164 Free PMC article.
Genetics of neonatal cardiomyopathy.
Towbin JA, Lipshultz SE. Towbin JA, et al. Curr Opin Cardiol. 1999 May;14(3):250-62. doi: 10.1097/00001573-199905000-00010. Curr Opin Cardiol. 1999. PMID: 10358797 Review.
The incidence of pediatric cardiomyopathy in two regions of the United States.
Lipshultz SE, Sleeper LA, Towbin JA, Lowe AM, Orav EJ, Cox GF, Lurie PR, McCoy KL, McDonald MA, Messere JE, Colan SD. Lipshultz SE, et al. Among authors: towbin ja. N Engl J Med. 2003 Apr 24;348(17):1647-55. doi: 10.1056/NEJMoa021715. N Engl J Med. 2003. PMID: 12711739 Free article.
Molecular genetics of heterotaxy syndromes.
Belmont JW, Mohapatra B, Towbin JA, Ware SM. Belmont JW, et al. Among authors: towbin ja. Curr Opin Cardiol. 2004 May;19(3):216-20. doi: 10.1097/00001573-200405000-00005. Curr Opin Cardiol. 2004. PMID: 15096953 Review.
544 results