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. |
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| 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 |
| FullText | Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 11590545 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti 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. – Name: Author Label: Authors Group: Au 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> – Name: TitleSource Label: Source Group: Src 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. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. – Name: TitleSource Label: Journal Info Group: Src 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 |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=11590545 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1086/324267 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 1033 Titles: – TitleFull: Nonmuscle myosin heavy chain IIA mutations define a spectrum of autosomal dominant macrothrombocytopenias: May-Hegglin anomaly and Fechtner, Sebastian, Epstein, and Alport-like syndromes. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Heath KE – PersonEntity: Name: NameFull: Campos-Barros A – PersonEntity: Name: NameFull: Toren A – PersonEntity: Name: NameFull: Rozenfeld-Granot G – PersonEntity: Name: NameFull: Carlsson LE – PersonEntity: Name: NameFull: Savige J – PersonEntity: Name: NameFull: Denison JC – PersonEntity: Name: NameFull: Gregory MC – PersonEntity: Name: NameFull: White JG – PersonEntity: Name: NameFull: Barker DF – PersonEntity: Name: NameFull: Greinacher A – PersonEntity: Name: NameFull: Epstein CJ – PersonEntity: Name: NameFull: Glucksman MJ – PersonEntity: Name: NameFull: Martignetti JA IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 11 Text: 2001 Nov Type: published Y: 2001 Identifiers: – Type: issn-print Value: 0002-9297 Numbering: – Type: volume Value: 69 – Type: issue Value: 5 Titles: – TitleFull: American journal of human genetics Type: main |
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