نتائج البحث - Alankarage, Dimuthu
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Functional characterization of a novel PBX1 de novo missense variant identified in a patient with syndromic congenital heart disease حسب Alankarage, Dimuthu, Szot, Justin O, Pachter, Nick, Slavotinek, Anne, Selleri, Licia, Shieh, Joseph T, Winlaw, David, Giannoulatou, Eleni, Chapman, Gavin, Dunwoodie, Sally L
منشور في 2020نص -
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Functional genomics and gene-environment interaction highlight the complexity of congenital heart disease caused by Notch pathway variants حسب Chapman, Gavin, Moreau, Julie L M, I P, Eddie, Szot, Justin O, Iyer, Kavitha R, Shi, Hongjun, Yam, Michelle X, O’Reilly, Victoria C, Enriquez, Annabelle, Greasby, Joelene A, Alankarage, Dimuthu, Martin, Ella M M A, Hanna, Bernadette C, Edwards, Matthew, Monger, Steven, Blue, Gillian M, Winlaw, David S, Ritchie, Helen E, Grieve, Stuart M, Giannoulatou, Eleni, Sparrow, Duncan B, Dunwoodie, Sally L
منشور في 2020نص