Resolving Differential Diagnostic Problems in von Willebrand Disease, in Fibrinogen Disorders, in Prekallikrein Deficiency and in Hereditary Hemorrhagic Telangiectasia by Next-Generation Sequencing

Gindele, RékaKerényi, AdrienneKállai, JuditPfliegler, GyörgySchlammadinger, ÁgotaSzegedi, IstvánMajor, TamásSzabó, ZsuzsannaBagoly, ZsuzsaKiss, CsongorKappelmayer, JánosBereczky, Zsuzsanna2021-03-182021-03-182021Life. -11 : 3 (2021), p. 1-23. -(cikkazonosító)202. -Life (Basel). - 2075-17292075-1729http://hdl.handle.net/2437/304324Resolving Differential Diagnostic Problems in von Willebrand Disease, in Fibrinogen Disorders, in Prekallikrein Deficiency and in Hereditary Hemorrhagic Telangiectasia by Next-Generation Sequencingfolyóiratcikkopen access journalhttp://webpac.lib.unideb.hu:8082/ebib/CorvinaWeb?action=cclfind&resultview=long&ccltext=idno+BIBFORM092499OrvostudományokKlinikai orvostudományokhttps://www.mdpi.com/2075-1729/11/3/202http://dx.doi.org/10.3390/life110302022022-04-12