Familial co-occurrence of congenital heart defects follows distinct patterns

por Ellesøe, Sabrina G, Workman, Christopher T, Bouvagnet, Patrice, Loffredo, Christopher A, McBride, Kim L, Hinton, Robert B, van Engelen, Klaartje, Gertsen, Emma C, Mulder, Barbara J M, Postma, Alex V, Anderson, Robert H, Hjortdal, Vibeke E, Brunak, Søren, Larsen, Lars A
Publicado 2018

Systems genetics analysis identifies calcium-signaling defects as novel cause of congenital heart disease

por Izarzugaza, Jose M. G., Ellesøe, Sabrina G., Doganli, Canan, Ehlers, Natasja Spring, Dalgaard, Marlene D., Audain, Enrique, Dombrowsky, Gregor, Banasik, Karina, Sifrim, Alejandro, Wilsdon, Anna, Thienpont, Bernard, Breckpot, Jeroen, Gewillig, Marc, Brook, J. David, Hitz, Marc-Phillip, Larsen, Lars A., Brunak, Søren
Publicado 2020