Next-Generation Sequencing (NGS)-Based Clinical Testing is Recommended for the Detection of Gene Mutations Associated with Familial Myelodysplastic Syndrome and Acute Myeloid Leukemia Predisposition Syndromes
2017 ◽
Vol 04
(03)
◽
2019 ◽
2019 ◽
2016 ◽
Vol 34
(15_suppl)
◽
pp. e18525-e18525
2016 ◽
2015 ◽
Vol 33
(15_suppl)
◽
pp. e18027-e18027
2018 ◽
Vol 36
(15_suppl)
◽
pp. 103-103
2018 ◽
Vol 36
(15_suppl)
◽
pp. 7051-7051
2020 ◽
Vol 26
(3)
◽
pp. S119-S120
2018 ◽
Vol 150
(suppl_1)
◽
pp. S154-S154