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High-throughput mut...
High-throughput mutational screening adds clinically important information in myelodysplastic syndromes and secondary or therapy-related acute myeloid leukemia.
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- Karimi, Mohsen (author)
- Karolinska Institutet
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- Nilsson, Christer (author)
- Karolinska Institutet
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- Dimitriou, Marios (author)
- Karolinska Institutet
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- Jansson, Monika (author)
- Karolinska Institutet
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- Matsson, Hans (author)
- Karolinska Institutet
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- Unneberg, Per (author)
- Stockholms universitet,Institutionen för biokemi och biofysik,Science for Life Laboratory (SciLifeLab)
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- Lehmann, Sören (author)
- Karolinska Institutet
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- Kere, Juha (author)
- Karolinska Institutet
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- Hellström-Lindberg, Eva (author)
- Karolinska Institutet
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(creator_code:org_t)
- 2015-03-13
- 2015
- English.
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In: Haematologica. - : Ferrata Storti Foundation (Haematologica). - 0390-6078 .- 1592-8721. ; 100:6, s. e223-5
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Subject headings
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Subject headings
- MEDICIN OCH HÄLSOVETENSKAP -- Medicinska och farmaceutiska grundvetenskaper -- Medicinsk genetik (hsv//swe)
- MEDICAL AND HEALTH SCIENCES -- Basic Medicine -- Medical Genetics (hsv//eng)
- NATURVETENSKAP -- Biologi (hsv//swe)
- NATURAL SCIENCES -- Biological Sciences (hsv//eng)
- MEDICIN OCH HÄLSOVETENSKAP -- Klinisk medicin -- Hematologi (hsv//swe)
- MEDICAL AND HEALTH SCIENCES -- Clinical Medicine -- Hematology (hsv//eng)
Keyword
- acute myeloid leukemia
- high-throughput mutational screening
- myelodysplastic syndromes
- secondary
- therapy-related
- Molekylär genetik
- Molecular Genetics
Publication and Content Type
- ref (subject category)
- art (subject category)
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