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Cryptic and partial deletions of PRDM16 and RUNX1 without t(1;21)(p36;q22) and/or RUNX1-PRDM16 fusion in a case of progressive chronic myeloid leukemia: A complex chromosomal rearrangement of underestimated frequency in disease progression?
- Published in:
- Genes, Chromosomes & Cancer, 2008, v. 47, n. 12, p. 1110, doi. 10.1002/gcc.20611
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- Article
Neurofibromatosis-1 gene deletions and mutations in de novo adult acute myeloid leukemia.
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- American Journal of Hematology, 2013, v. 88, n. 4, p. 306, doi. 10.1002/ajh.23403
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- Article
Detection of a new heterozygous germline ETV6 mutation in a case with hyperdiploid acute lymphoblastic leukemia.
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- European Journal of Haematology, 2018, v. 100, n. 1, p. 104, doi. 10.1111/ejh.12981
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- Article
Familial occurrence of thymoma and autoimmune diseases with the constitutional translocation t(14;20)(q24.1;p12.3).
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- Genes, Chromosomes & Cancer, 2005, v. 44, n. 2, p. 154
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- Article
MYD88 L265P mutation contributes to the diagnosis of Bing Neel syndrome.
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- British Journal of Haematology, 2014, v. 167, n. 4, p. 506, doi. 10.1111/bjh.13078
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- Article
Publisher Correction: Frugal alignment-free identification of FLT3-internal tandem duplications with FiLT3r.
- Published in:
- 2022
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- Correction Notice
Frugal alignment-free identification of FLT3-internal tandem duplications with FiLT3r.
- Published in:
- BMC Bioinformatics, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s12859-022-05079-x
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- Article
Frugal alignment-free identification of FLT3-internal tandem duplications with FiLT3r.
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- BMC Bioinformatics, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s12859-022-04983-6
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- Publication type:
- Article
Clinico-Biological Features and Clonal Hematopoiesis in Patients with Severe COVID-19.
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- Cancers, 2020, v. 12, n. 7, p. 1992, doi. 10.3390/cancers12071992
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- Article
Clofarabine Improves Relapse-Free Survival of Acute Myeloid Leukemia in Younger Adults with Micro-Complex Karyotype.
- Published in:
- Cancers, 2020, v. 12, n. 1, p. 88, doi. 10.3390/cancers12010088
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- Article