Exome sequencing identifies a rare HSPG2 variant associated with familial idiopathic scoliosis.
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| Title: | Exome sequencing identifies a rare HSPG2 variant associated with familial idiopathic scoliosis. |
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| Authors: | Baschal EE; Department of Orthopedics, University of Colorado Denver Anschutz Medical Campus, Aurora, Colorado, 80045., Wethey CI; Department of Orthopedics, University of Colorado Denver Anschutz Medical Campus, Aurora, Colorado, 80045., Swindle K; Department of Orthopedics, University of Colorado Denver Anschutz Medical Campus, Aurora, Colorado, 80045., Baschal RM; Musculoskeletal Research Center, Children's Hospital Colorado, Aurora, Colorado, 80045., Gowan K; Department of Biochemistry, University of Colorado Denver Anschutz Medical Campus, Aurora, Colorado, 80045., Tang NL; Department of Chemical Pathology and Li Ka Shing Institute of Health Sciences, Faculty of Medicine, The Chinese University of Hong Kong, Hong Kong SAR., Alvarado DM; Department of Orthopaedic Surgery, Washington University School of Medicine, St. Louis, Missouri, 63130., Haller GE; Department of Orthopaedic Surgery, Washington University School of Medicine, St. Louis, Missouri, 63130., Dobbs MB; Department of Orthopaedic Surgery, Washington University School of Medicine, St. Louis, Missouri, 63130 Saint Louis Shriners Hospital for Children, St. Louis, Missouri, 63131., Taylor MR; Department of Cardiology, University of Colorado Denver Anschutz Medical Campus, Aurora, Colorado, 80045., Gurnett CA; Department of Orthopaedic Surgery, Washington University School of Medicine, St. Louis, Missouri, 63130 Department of Neurology, Washington University School of Medicine, St. Louis, Missouri, 63130., Jones KL; Department of Biochemistry, University of Colorado Denver Anschutz Medical Campus, Aurora, Colorado, 80045., Miller NH; Department of Orthopedics, University of Colorado Denver Anschutz Medical Campus, Aurora, Colorado, 80045 Musculoskeletal Research Center, Children's Hospital Colorado, Aurora, Colorado, 80045 Nancy.Hadley-Miller@ucdenver.edu. |
| Source: | G3 (Bethesda, Md.) [G3 (Bethesda)] 2014 Dec 12; Vol. 5 (2), pp. 167-74. Date of Electronic Publication: 2014 Dec 12. |
| Publication Type: | Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: Oxford University Press Country of Publication: England NLM ID: 101566598 Publication Model: Electronic Cited Medium: Internet ISSN: 2160-1836 (Electronic) Linking ISSN: 21601836 NLM ISO Abbreviation: G3 (Bethesda) Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
| FullText | Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 25504735 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Exome sequencing identifies a rare HSPG2 variant associated with familial idiopathic scoliosis. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Baschal+EE%22">Baschal EE</searchLink>; Department of Orthopedics, University of Colorado Denver Anschutz Medical Campus, Aurora, Colorado, 80045.<br /><searchLink fieldCode="AU" term="%22Wethey+CI%22">Wethey CI</searchLink>; Department of Orthopedics, University of Colorado Denver Anschutz Medical Campus, Aurora, Colorado, 80045.<br /><searchLink fieldCode="AU" term="%22Swindle+K%22">Swindle K</searchLink>; Department of Orthopedics, University of Colorado Denver Anschutz Medical Campus, Aurora, Colorado, 80045.<br /><searchLink fieldCode="AU" term="%22Baschal+RM%22">Baschal RM</searchLink>; Musculoskeletal Research Center, Children's Hospital Colorado, Aurora, Colorado, 80045.<br /><searchLink fieldCode="AU" term="%22Gowan+K%22">Gowan K</searchLink>; Department of Biochemistry, University of Colorado Denver Anschutz Medical Campus, Aurora, Colorado, 80045.<br /><searchLink fieldCode="AU" term="%22Tang+NL%22">Tang NL</searchLink>; Department of Chemical Pathology and Li Ka Shing Institute of Health Sciences, Faculty of Medicine, The Chinese University of Hong Kong, Hong Kong SAR.<br /><searchLink fieldCode="AU" term="%22Alvarado+DM%22">Alvarado DM</searchLink>; Department of Orthopaedic Surgery, Washington University School of Medicine, St. Louis, Missouri, 63130.<br /><searchLink fieldCode="AU" term="%22Haller+GE%22">Haller GE</searchLink>; Department of Orthopaedic Surgery, Washington University School of Medicine, St. Louis, Missouri, 63130.<br /><searchLink fieldCode="AU" term="%22Dobbs+MB%22">Dobbs MB</searchLink>; Department of Orthopaedic Surgery, Washington University School of Medicine, St. Louis, Missouri, 63130 Saint Louis Shriners Hospital for Children, St. Louis, Missouri, 63131.<br /><searchLink fieldCode="AU" term="%22Taylor+MR%22">Taylor MR</searchLink>; Department of Cardiology, University of Colorado Denver Anschutz Medical Campus, Aurora, Colorado, 80045.<br /><searchLink fieldCode="AU" term="%22Gurnett+CA%22">Gurnett CA</searchLink>; Department of Orthopaedic Surgery, Washington University School of Medicine, St. Louis, Missouri, 63130 Department of Neurology, Washington University School of Medicine, St. Louis, Missouri, 63130.<br /><searchLink fieldCode="AU" term="%22Jones+KL%22">Jones KL</searchLink>; Department of Biochemistry, University of Colorado Denver Anschutz Medical Campus, Aurora, Colorado, 80045.<br /><searchLink fieldCode="AU" term="%22Miller+NH%22">Miller NH</searchLink>; Department of Orthopedics, University of Colorado Denver Anschutz Medical Campus, Aurora, Colorado, 80045 Musculoskeletal Research Center, Children's Hospital Colorado, Aurora, Colorado, 80045 Nancy.Hadley-Miller@ucdenver.edu. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22101566598%22">G3 (Bethesda, Md.)</searchLink> [G3 (Bethesda)] 2014 Dec 12; Vol. 5 (2), pp. 167-74. <i>Date of Electronic Publication: </i>2014 Dec 12. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't – 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>England <i>NLM ID: </i>101566598 <i>Publication Model: </i>Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>2160-1836 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2221601836%22">21601836 </searchLink><i>NLM ISO Abbreviation: </i>G3 (Bethesda) <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=25504735 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1534/g3.114.015669 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 167 Titles: – TitleFull: Exome sequencing identifies a rare HSPG2 variant associated with familial idiopathic scoliosis. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Baschal EE – PersonEntity: Name: NameFull: Wethey CI – PersonEntity: Name: NameFull: Swindle K – PersonEntity: Name: NameFull: Baschal RM – PersonEntity: Name: NameFull: Gowan K – PersonEntity: Name: NameFull: Tang NL – PersonEntity: Name: NameFull: Alvarado DM – PersonEntity: Name: NameFull: Haller GE – PersonEntity: Name: NameFull: Dobbs MB – PersonEntity: Name: NameFull: Taylor MR – PersonEntity: Name: NameFull: Gurnett CA – PersonEntity: Name: NameFull: Jones KL – PersonEntity: Name: NameFull: Miller NH IsPartOfRelationships: – BibEntity: Dates: – D: 12 M: 12 Text: 2014 Dec 12 Type: published Y: 2014 Identifiers: – Type: issn-electronic Value: 2160-1836 Numbering: – Type: volume Value: 5 – Type: issue Value: 2 Titles: – TitleFull: G3 (Bethesda, Md.) Type: main |
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