Genetic Variants in Isolated Ebstein Anomaly Implicated in Myocardial Development Pathways

Por Sicko, Robert J., Browne, Marilyn L., Rigler, Shannon L., Druschel, Charlotte M., Liu, Gang, Fan, Ruzong, Romitti, Paul A., Caggana, Michele, Kay, Denise M., Brody, Lawrence C., Mills, James L.
Publicado no PLoS One (2016)

Rare Copy Number Variants in a Population Based Investigation of Hypoplastic Right Heart Syndrome

Por Dimopoulos, Aggeliki, Sicko, Robert J., Kay, Denise M., Rigler, Shannon L., Druschel, Charlotte M., Caggana, Michele, Browne, Marilyn L., Fan, Ruzong, Romitti, Paul A., Brody, Lawrence C., Mills, James L.
Publicado no Birth Defects Res (2017)

Copy-number variant analysis of classic heterotaxy highlights the importance of body patterning pathways

Por Hagen, Erin M., Sicko, Robert J., Kay, Denise M., Rigler, Shannon L., Dimopoulos, Aggeliki, Ahmad, Shabbir, Doleman, Margaret H., Fan, Ruzong, Romitti, Paul A., Browne, Marilyn L., Caggana, Michele, Brody, Lawrence C., Shaw, Gary M., Jelliffe-Pawlowski, Laura L., Mills, James L.
Publicado no Hum Genet (2016)