Zobrazeno 1 - 1
of 1
pro vyhledávání: '"Duowen Huang"'
Publikováno v:
BMC Pediatrics, Vol 24, Iss 1, Pp 1-6 (2024)
Abstract Radioulnar synostosis with amegakaryocytic thrombocytopenia (RUSAT) type 2, caused by MDS1 and EVI1 complex locus (MECOM) gene mutations, is a rare inherited bone marrow failure syndrome (IBMFS) with skeletal anomalies, characterized by vary
Externí odkaz:
https://doaj.org/article/3cd23bedd0e34238ac949dd28c0cd7c5
