Holt–Oram syndrome with intermediate atrioventricular canal defect, and aortic coarctation: Functional characterization of a de novo TBX5 mutation

查看全文 作　　者：Anwar;Baban;Letizia;Pitto;Silvia;Pulignani;Monica;Cresci;Laura;Mariani;Carolina;Gambacciani;Maria;Cristina;Digilio;Giacomo;Pongiglione;Sonia;Albanese 出　　处：《Am. J. Med. Genet》索引2014年第6期,共0页