S. Parks

发表

Coding Sequence Mutations Identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 Patients with Familial or Idiopathic Dilated Cardiomyopathy

R. Hershberger, P. Jakobs, D. Nauman, 2008, Clinical and translational science.

Mutations of presenilin genes in dilated cardiomyopathy and heart failure.

Michael Litt, R. Hershberger, C. Allen, 2006, American journal of human genetics.

Real-time polymerase chain reaction with fluorescent hybridization probes for the detection of prevalent mutations causing common thrombophilic and iron overload phenotypes.

B. Popovich, R. Press, S. Parks, 2001, American journal of clinical pathology.

Clinical and Functional Characterization of TNNT2 Mutations Identified in Patients With Dilated Cardiomyopathy

J. Potter, R. Hershberger, Duanxiang Li, 2009, Circulation. Cardiovascular genetics.

Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results

R. Ries, R. Press, P. Gomez, 1999, Nature Genetics.

Lamin A/C mutation analysis in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy.

P. Rahko, R. Hershberger, P. Jakobs, 2008, American heart journal.

Diagnostic Molecular Pathology

R. Press, S. Parks, James Huang, 2006 .

Clinical characteristics of 304 kindreds evaluated for familial dilated cardiomyopathy.

R. Hershberger, G. Pantely, D. Nauman, 2006, Journal of cardiac failure.

Clinical Investigations Clinical Characteristics of 304 Kindreds Evaluated for Familial Dilated Cardiomyopathy

R. Hershberger, G. Pantely, D. Nauman, 2006 .