Nonmuscle myosin heavy chain IIA mutations define a spectrum of autosomal dominant macrothrombocytopenias: May-Hegglin anomaly and Fechtner, Sebastian, Epstein, and Alport-like syndromes.

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Title: Nonmuscle myosin heavy chain IIA mutations define a spectrum of autosomal dominant macrothrombocytopenias: May-Hegglin anomaly and Fechtner, Sebastian, Epstein, and Alport-like syndromes.
Authors: Heath KE; Department of Human Genetics, Mount Sinai School of Medicine, New York, NY 10029, USA., Campos-Barros A, Toren A, Rozenfeld-Granot G, Carlsson LE, Savige J, Denison JC, Gregory MC, White JG, Barker DF, Greinacher A, Epstein CJ, Glucksman MJ, Martignetti JA
Source: American journal of human genetics [Am J Hum Genet] 2001 Nov; Vol. 69 (5), pp. 1033-45. Date of Electronic Publication: 2001 Oct 04.
Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
Journal Info: Publisher: Cell Press Country of Publication: United States NLM ID: 0370475 Publication Model: Print-Electronic Cited Medium: Print ISSN: 0002-9297 (Print) Linking ISSN: 00029297 NLM ISO Abbreviation: Am J Hum Genet Subsets: MEDLINE
Database: MEDLINE Ultimate
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PubType: Academic Journal
PubTypeId: academicJournal
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  Data: Nonmuscle myosin heavy chain IIA mutations define a spectrum of autosomal dominant macrothrombocytopenias: May-Hegglin anomaly and Fechtner, Sebastian, Epstein, and Alport-like syndromes.
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  Data: <searchLink fieldCode="AU" term="%22Heath+KE%22">Heath KE</searchLink>; Department of Human Genetics, Mount Sinai School of Medicine, New York, NY 10029, USA.<br /><searchLink fieldCode="AU" term="%22Campos-Barros+A%22">Campos-Barros A</searchLink><br /><searchLink fieldCode="AU" term="%22Toren+A%22">Toren A</searchLink><br /><searchLink fieldCode="AU" term="%22Rozenfeld-Granot+G%22">Rozenfeld-Granot G</searchLink><br /><searchLink fieldCode="AU" term="%22Carlsson+LE%22">Carlsson LE</searchLink><br /><searchLink fieldCode="AU" term="%22Savige+J%22">Savige J</searchLink><br /><searchLink fieldCode="AU" term="%22Denison+JC%22">Denison JC</searchLink><br /><searchLink fieldCode="AU" term="%22Gregory+MC%22">Gregory MC</searchLink><br /><searchLink fieldCode="AU" term="%22White+JG%22">White JG</searchLink><br /><searchLink fieldCode="AU" term="%22Barker+DF%22">Barker DF</searchLink><br /><searchLink fieldCode="AU" term="%22Greinacher+A%22">Greinacher A</searchLink><br /><searchLink fieldCode="AU" term="%22Epstein+CJ%22">Epstein CJ</searchLink><br /><searchLink fieldCode="AU" term="%22Glucksman+MJ%22">Glucksman MJ</searchLink><br /><searchLink fieldCode="AU" term="%22Martignetti+JA%22">Martignetti JA</searchLink>
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  Data: <searchLink fieldCode="JN" term="%220370475%22">American journal of human genetics</searchLink> [Am J Hum Genet] 2001 Nov; Vol. 69 (5), pp. 1033-45. <i>Date of Electronic Publication: </i>2001 Oct 04.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Cell+Press%22">Cell Press </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>0370475 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Print <i>ISSN: </i>0002-9297 (Print) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2200029297%22">00029297 </searchLink><i>NLM ISO Abbreviation: </i>Am J Hum Genet <i>Subsets: </i>MEDLINE
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        Value: 10.1086/324267
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        Text: English
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              Text: 2001 Nov
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