Genomic regions associated with microdeletion/microduplication syndromes exhibit extreme diversity of structural variation.
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| Title: | Genomic regions associated with microdeletion/microduplication syndromes exhibit extreme diversity of structural variation. |
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| Authors: | Mostovoy Y; Cardiovascular Research Institute, UCSF School of Medicine, San Francisco, CA 94143, USA., Yilmaz F; Department of Integrative Biology, University of Colorado Denver, Denver, CO 80204, USA.; Department of Pediatrics, Section of Clinical Genetics and Metabolism, University of Colorado School of Medicine, Aurora, CO 80045, USA., Chow SK; Cardiovascular Research Institute, UCSF School of Medicine, San Francisco, CA 94143, USA., Chu C; Cardiovascular Research Institute, UCSF School of Medicine, San Francisco, CA 94143, USA., Lin C; Cardiovascular Research Institute, UCSF School of Medicine, San Francisco, CA 94143, USA., Geiger EA; Department of Pediatrics, Section of Clinical Genetics and Metabolism, University of Colorado School of Medicine, Aurora, CO 80045, USA., Meeks NJL; Department of Pediatrics, Section of Clinical Genetics and Metabolism, University of Colorado School of Medicine, Aurora, CO 80045, USA., Chatfield KC; Department of Pediatrics, Section of Clinical Genetics and Metabolism, University of Colorado School of Medicine, Aurora, CO 80045, USA.; Department of Pediatrics, Section of Cardiology, University of Colorado School of Medicine, Aurora, CO 80045, USA., Coughlin CR; Department of Pediatrics, Section of Clinical Genetics and Metabolism, University of Colorado School of Medicine, Aurora, CO 80045, USA., Surti U; Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213, USA., Kwok PY; Cardiovascular Research Institute, UCSF School of Medicine, San Francisco, CA 94143, USA.; Department of Dermatology, UCSF School of Medicine, San Francisco, CA 94143, USA.; Institute for Human Genetics, UCSF School of Medicine, San Francisco, CA 94143, USA., Shaikh TH; Department of Pediatrics, Section of Clinical Genetics and Metabolism, University of Colorado School of Medicine, Aurora, CO 80045, USA. |
| Source: | Genetics [Genetics] 2021 Feb 09; Vol. 217 (2). |
| Publication Type: | Journal Article; Research Support, N.I.H., Extramural |
| Journal Info: | Publisher: Oxford University Press Country of Publication: United States NLM ID: 0374636 Publication Model: Print Cited Medium: Internet ISSN: 1943-2631 (Electronic) Linking ISSN: 00166731 NLM ISO Abbreviation: Genetics Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
| FullText | Links: – Type: pdflink Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 33724415 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Genomic regions associated with microdeletion/microduplication syndromes exhibit extreme diversity of structural variation. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Mostovoy+Y%22">Mostovoy Y</searchLink>; Cardiovascular Research Institute, UCSF School of Medicine, San Francisco, CA 94143, USA.<br /><searchLink fieldCode="AU" term="%22Yilmaz+F%22">Yilmaz F</searchLink>; Department of Integrative Biology, University of Colorado Denver, Denver, CO 80204, USA.; Department of Pediatrics, Section of Clinical Genetics and Metabolism, University of Colorado School of Medicine, Aurora, CO 80045, USA.<br /><searchLink fieldCode="AU" term="%22Chow+SK%22">Chow SK</searchLink>; Cardiovascular Research Institute, UCSF School of Medicine, San Francisco, CA 94143, USA.<br /><searchLink fieldCode="AU" term="%22Chu+C%22">Chu C</searchLink>; Cardiovascular Research Institute, UCSF School of Medicine, San Francisco, CA 94143, USA.<br /><searchLink fieldCode="AU" term="%22Lin+C%22">Lin C</searchLink>; Cardiovascular Research Institute, UCSF School of Medicine, San Francisco, CA 94143, USA.<br /><searchLink fieldCode="AU" term="%22Geiger+EA%22">Geiger EA</searchLink>; Department of Pediatrics, Section of Clinical Genetics and Metabolism, University of Colorado School of Medicine, Aurora, CO 80045, USA.<br /><searchLink fieldCode="AU" term="%22Meeks+NJL%22">Meeks NJL</searchLink>; Department of Pediatrics, Section of Clinical Genetics and Metabolism, University of Colorado School of Medicine, Aurora, CO 80045, USA.<br /><searchLink fieldCode="AU" term="%22Chatfield+KC%22">Chatfield KC</searchLink>; Department of Pediatrics, Section of Clinical Genetics and Metabolism, University of Colorado School of Medicine, Aurora, CO 80045, USA.; Department of Pediatrics, Section of Cardiology, University of Colorado School of Medicine, Aurora, CO 80045, USA.<br /><searchLink fieldCode="AU" term="%22Coughlin+CR%22">Coughlin CR</searchLink>; Department of Pediatrics, Section of Clinical Genetics and Metabolism, University of Colorado School of Medicine, Aurora, CO 80045, USA.<br /><searchLink fieldCode="AU" term="%22Surti+U%22">Surti U</searchLink>; Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213, USA.<br /><searchLink fieldCode="AU" term="%22Kwok+PY%22">Kwok PY</searchLink>; Cardiovascular Research Institute, UCSF School of Medicine, San Francisco, CA 94143, USA.; Department of Dermatology, UCSF School of Medicine, San Francisco, CA 94143, USA.; Institute for Human Genetics, UCSF School of Medicine, San Francisco, CA 94143, USA.<br /><searchLink fieldCode="AU" term="%22Shaikh+TH%22">Shaikh TH</searchLink>; Department of Pediatrics, Section of Clinical Genetics and Metabolism, University of Colorado School of Medicine, Aurora, CO 80045, USA. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%220374636%22">Genetics</searchLink> [Genetics] 2021 Feb 09; Vol. 217 (2). – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article; Research Support, N.I.H., Extramural – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Oxford+University+Press%22">Oxford University Press </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>0374636 <i>Publication Model: </i>Print <i>Cited Medium: </i>Internet <i>ISSN: </i>1943-2631 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2200166731%22">00166731 </searchLink><i>NLM ISO Abbreviation: </i>Genetics <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=33724415 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1093/genetics/iyaa038 Languages: – Code: eng Text: English Titles: – TitleFull: Genomic regions associated with microdeletion/microduplication syndromes exhibit extreme diversity of structural variation. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Mostovoy Y – PersonEntity: Name: NameFull: Yilmaz F – PersonEntity: Name: NameFull: Chow SK – PersonEntity: Name: NameFull: Chu C – PersonEntity: Name: NameFull: Lin C – PersonEntity: Name: NameFull: Geiger EA – PersonEntity: Name: NameFull: Meeks NJL – PersonEntity: Name: NameFull: Chatfield KC – PersonEntity: Name: NameFull: Coughlin CR – PersonEntity: Name: NameFull: Surti U – PersonEntity: Name: NameFull: Kwok PY – PersonEntity: Name: NameFull: Shaikh TH IsPartOfRelationships: – BibEntity: Dates: – D: 09 M: 02 Text: 2021 Feb 09 Type: published Y: 2021 Identifiers: – Type: issn-electronic Value: 1943-2631 Numbering: – Type: volume Value: 217 – Type: issue Value: 2 Titles: – TitleFull: Genetics Type: main |
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