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Clinical and Translational Science|May 5, 2009
Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathyRay E Hershberger, Sharie B Parks, Jessica D Kushner, et al.The Journal of Foot Surgery|January 1, 1984
Solitary osteochondroma of the foot: an in-depth study with case reportsC O Fuselier, T Binning, D Kushner, et al.Journal of Genetic Counseling|August 14, 2012
Return of genetic results in the familial dilated cardiomyopathy research projectJill D Siegfried, Ana Morales, Jessica D Kushner, et al.Circulation. Cardiovascular Genetics|December 25, 2009
Clinical and functional characterization of TNNT2 mutations identified in patients with dilated cardiomyopathyRay E Hershberger, Jose Renato Pinto, Sharie B Parks, et al.American Heart Journal|July 1, 2008
Lamin A/C mutation analysis in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathySharie B Parks, Jessica D Kushner, Deirdre Nauman, et al.Clinical Genetics|September 8, 2022
Six new cases of CRB2-related syndrome and a review of clinical findings in 28 reported patientsMichelle Adutwum, Anna Hurst, Ghayda Mirzaa, et al.American Journal of Human Genetics|December 23, 2006
Mutations of presenilin genes in dilated cardiomyopathy and heart failureDuanxiang Li, Sharie B Parks, Jessica D Kushner, et al.Journal of Genetic Counseling|March 12, 2017
At the Heart of the Pregnancy: What Prenatal and Cardiovascular Genetic Counselors Need to Know about Maternal Heart DiseaseAna Morales, Dawn C Allain, Patricia Arscott, et al.Pageof 5