Allele-specific methylation of a functional CTCF binding site upstream of MEG3 in the human imprinted domain of 14q32 by Rosa, Alberto L, Wu, Yuan-Qing, Kwabi-Addo, Bernard, Coveler, Karen J, Reid Sutton, V, Shaffer, Lisa G

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Mutations in the muscle LIM protein and α-actinin-2 genes in dilated cardiomyopathy and endocardial fibroelastosis by Mohapatra, Bhagyalaxmi, Jimenez, Shinawe, Lin, Jiuann Huey, Bowles, Karla R, Coveler, Karen J, Marx, Joseph G, Chrisco, Michele A, Murphy, Ross T, Lurie, Paul R, Schwartz, Robert J, Elliott, Perry M, Vatta, Matteo, McKenna, William, Towbin, Jeffrey A, Bowles, Neil E

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Isolated left ventricular noncompaction is rarely caused by mutations in G4.5, α- dystrobrevin and FK Binding Protein-12 by Kenton, Alexander B, Sanchez, Ximena, Coveler, Karen J, Makar, Kimberly A, Jimenez, Shinawe, Ichida, Fukiko, Murphy, Ross T, Elliott, Perry M, McKenna, William, Bowles, Neil E, Towbin, Jeffrey A, Bowles, Karla R

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A case of segmental paternal isodisomy of chromosome 14 by COVELER, Karen J, YANG, Sam P, REID SUTTON, V, MILSTEIN, Jay M, WU, Yuan-Qing, KNOX-DU BOIS, Cami, BEISCHEL, Linda S, JOHNSON, John P, SHAFFER, Lisa G

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Beyond the exome: What’s next in diagnostic testing for Mendelian conditions by Wojcik, Monica H., Reuter, Chloe M., Marwaha, Shruti, Mahmoud, Medhat, Duyzend, Michael H., Barseghyan, Hayk, Yuan, Bo, Boone, Philip M., Groopman, Emily E., Délot, Emmanuèle C., Jain, Deepti, Sanchis-Juan, Alba, Starita, Lea M., Talkowski, Michael, Montgomery, Stephen B., Bamshad, Michael J., Chong, Jessica X., Wheeler, Matthew T., Berger, Seth I., O'Donnell-Luria, Anne, Sedlazeck, Fritz J., Miller, Danny E.

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