Found: 7
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Juvenile hemochromatosis due to homozygosity for the G320V mutation in the HJV gene with fatal outcome.
- Published in:
- Clinical Genetics, 2009, v. 76, n. 5, p. 493, doi. 10.1111/j.1399-0004.2009.01261.x
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- Publication type:
- Article
Testing the parents to confirm genotypes of CF patients is highly recommended: report of two cases.
- Published in:
- European Journal of Human Genetics, 2009, v. 17, n. 4, p. 417, doi. 10.1038/ejhg.2008.190
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- Publication type:
- Article
B-CLL developing in a patient with PV is not affected by V617F mutation of the Janus kinase 2.
- Published in:
- 2006
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- Publication type:
- Letter
Different involvement of the megakaryocytic lineage by the JAK2<sup>V617F</sup> mutation in Polycythemia vera, essential thrombocythemia and chronic idiopathic myelofibrosis.
- Published in:
- Annals of Hematology, 2007, v. 86, n. 4, p. 245, doi. 10.1007/s00277-007-0252-3
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- Publication type:
- Article
Role of epigenetic changes in hematological malignancies.
- Published in:
- Annals of Hematology, 2004, v. 83, n. 3, p. 137, doi. 10.1007/s00277-003-0798-7
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- Publication type:
- Article
Hypermethylation of the suppressor of cytokine signalling-1 ( SOCS-1) in myelodysplastic syndrome.
- Published in:
- British Journal of Haematology, 2005, v. 130, n. 2, p. 209, doi. 10.1111/j.1365-2141.2005.05590.x
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- Publication type:
- Article
Epigenetic defects of hepatocellular carcinoma are already found in non-neoplastic liver cells from patients with hereditary haemochromatosis.
- Published in:
- Human Molecular Genetics, 2007, v. 16, n. 11, p. 1335, doi. 10.1093/hmg/ddm082
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- Publication type:
- Article