Detalhe da pesquisa
1.
Comprehensive whole-genome sequencing of an early-stage primary myelofibrosis patient defines low mutational burden and non-recurrent candidate genes.
Haematologica
; 98(11): 1689-96, 2013 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-23872309
2.
A novel splice donor mutation in the thrombopoietin gene leads to exon 2 skipping in a Filipino family with hereditary thrombocythemia.
Blood
; 118(26): 6988-90, 2011 Dec 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-22194398
3.
Implementation of a timed, electronic, assessment-driven potassium-replacement protocol.
Am J Health Syst Pharm
; 74(12): 927-931, 2017 Jun 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-28487284