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Mutations in SETBP1 are recurrent in myelodysplastic syndromes and often coexist with cytogenetic markers associated with disease progression.

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Title: Mutations in SETBP1 are recurrent in myelodysplastic syndromes and often coexist with cytogenetic markers associated with disease progression.
Authors: Fernandez-Mercado M; LLR Molecular Haematology Unit, NDCLS, RDM, John Radcliffe Hospital, Oxford, UK., Pellagatti A, Di Genua C, Larrayoz MJ, Winkelmann N, Aranaz P, Burns A, Schuh A, Calasanz MJ, Cross NC, Boultwood J
Source: British journal of haematology [Br J Haematol] 2013 Oct; Vol. 163 (2), pp. 235-9. Date of Electronic Publication: 2013 Jul 24.
Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Wiley-Blackwell Country of Publication: England NLM ID: 0372544 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1365-2141 (Electronic) Linking ISSN: 00071048 NLM ISO Abbreviation: Br J Haematol Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: Mutations in SETBP1 are recurrent in myelodysplastic syndromes and often coexist with cytogenetic markers associated with disease progression.
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  Data: <searchLink fieldCode="AU" term="%22Fernandez-Mercado+M%22">Fernandez-Mercado M</searchLink>; LLR Molecular Haematology Unit, NDCLS, RDM, John Radcliffe Hospital, Oxford, UK.<br /><searchLink fieldCode="AU" term="%22Pellagatti+A%22">Pellagatti A</searchLink><br /><searchLink fieldCode="AU" term="%22Di+Genua+C%22">Di Genua C</searchLink><br /><searchLink fieldCode="AU" term="%22Larrayoz+MJ%22">Larrayoz MJ</searchLink><br /><searchLink fieldCode="AU" term="%22Winkelmann+N%22">Winkelmann N</searchLink><br /><searchLink fieldCode="AU" term="%22Aranaz+P%22">Aranaz P</searchLink><br /><searchLink fieldCode="AU" term="%22Burns+A%22">Burns A</searchLink><br /><searchLink fieldCode="AU" term="%22Schuh+A%22">Schuh A</searchLink><br /><searchLink fieldCode="AU" term="%22Calasanz+MJ%22">Calasanz MJ</searchLink><br /><searchLink fieldCode="AU" term="%22Cross+NC%22">Cross NC</searchLink><br /><searchLink fieldCode="AU" term="%22Boultwood+J%22">Boultwood J</searchLink>
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  Data: <searchLink fieldCode="JN" term="%220372544%22">British journal of haematology</searchLink> [Br J Haematol] 2013 Oct; Vol. 163 (2), pp. 235-9. <i>Date of Electronic Publication: </i>2013 Jul 24.
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  Data: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Wiley-Blackwell%22">Wiley-Blackwell </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>0372544 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1365-2141 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2200071048%22">00071048 </searchLink><i>NLM ISO Abbreviation: </i>Br J Haematol <i>Subsets: </i>MEDLINE
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        Value: 10.1111/bjh.12491
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        Text: English
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      – TitleFull: Mutations in SETBP1 are recurrent in myelodysplastic syndromes and often coexist with cytogenetic markers associated with disease progression.
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              Text: 2013 Oct
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