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THSD1 (Thrombospondin Type 1 Domain Containing Protein 1) Mutation in the Pathogenesis of Intracranial Aneurysm and Subarachnoid Hemorrhage.
Santiago-Sim T, Fang X, Hennessy ML, Nalbach SV, DePalma SR, Lee MS, Greenway SC, McDonough B, Hergenroeder GW, Patek KJ, Colosimo SM, Qualmann KJ, Hagan JP, Milewicz DM, MacRae CA, Dymecki SM, Seidman CE, Seidman JG, Kim DH. Santiago-Sim T, et al. Among authors: seidman jg, seidman ce. Stroke. 2016 Dec;47(12):3005-3013. doi: 10.1161/STROKEAHA.116.014161. Epub 2016 Nov 15. Stroke. 2016. PMID: 27895300 Free PMC article.
Phenotypic diversity in hypertrophic cardiomyopathy.
Arad M, Seidman JG, Seidman CE. Arad M, et al. Among authors: seidman jg, seidman ce. Hum Mol Genet. 2002 Oct 1;11(20):2499-506. doi: 10.1093/hmg/11.20.2499. Hum Mol Genet. 2002. PMID: 12351586 Review.
Novel locus for an inherited cardiomyopathy maps to chromosome 7.
Song L, DePalma SR, Kharlap M, Zenovich AG, Cirino A, Mitchell R, McDonough B, Maron BJ, Seidman CE, Seidman JG, Ho CY. Song L, et al. Among authors: seidman jg, seidman ce. Circulation. 2006 May 9;113(18):2186-92. doi: 10.1161/CIRCULATIONAHA.106.615658. Epub 2006 May 1. Circulation. 2006. PMID: 16651466
A nonsense mutation in MSX1 causes Witkop syndrome.
Jumlongras D, Bei M, Stimson JM, Wang WF, DePalma SR, Seidman CE, Felbor U, Maas R, Seidman JG, Olsen BR. Jumlongras D, et al. Among authors: seidman jg, seidman ce. Am J Hum Genet. 2001 Jul;69(1):67-74. doi: 10.1086/321271. Epub 2001 May 16. Am J Hum Genet. 2001. PMID: 11369996 Free PMC article.
The coming of age of cardiovascular science.
Seidman CE, Seidman JG. Seidman CE, et al. Among authors: seidman jg. Cold Spring Harb Symp Quant Biol. 2002;67:543-50. doi: 10.1101/sqb.2002.67.543. Cold Spring Harb Symp Quant Biol. 2002. PMID: 12858581 No abstract available.
578 results