论文信息 - Congenital asplenia in mice and humans with mutations in a Pbx/Nkx2-5/p15 module. - 字舞流文

Congenital asplenia in mice and humans with mutations in a Pbx/Nkx2-5/p15 module.

J. Casanova | D. Elliott | T. Capellini | C. Hidaka | O. Prall | R. Harvey | C. Chang | B. Boisson | A. Bolze | N. Mahlaoui | L. Selleri | M. Saggese | A. Brendolan | Matthew Koss | M. Solloway | Mark J. Solloway | E. Lenti | Ekaterina Bojilova