Genetic variants in FBLIM1 gene do not contribute to SAPHO syndrome and chronic recurrent multifocal osteomyelitis in typical patient groups.
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| Title: | Genetic variants in FBLIM1 gene do not contribute to SAPHO syndrome and chronic recurrent multifocal osteomyelitis in typical patient groups. |
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| Authors: | Assmann, Gunter1 (AUTHOR), Köhm, Michaela2 (AUTHOR), Schuster, Volker3 (AUTHOR), Behrens, Frank2 (AUTHOR), Mössner, Rotraut4 (AUTHOR), Magnolo, Nina5 (AUTHOR), Oji, Vinzenz5 (AUTHOR), Burkhardt, Harald2 (AUTHOR), Hüffmeier, Ulrike6 (AUTHOR) ulrike.hueffmeier@uk-erlangen.de |
| Source: | BMC Medical Genetics. 5/12/2020, Vol. 21 Issue 1, p1-7. 7p. |
| Database: | Academic Search Ultimate |
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| FullText | Links: – Type: pdflink Text: Availability: 1 |
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| Header | DbId: asn DbLabel: Academic Search Ultimate An: 143169279 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Genetic variants in FBLIM1 gene do not contribute to SAPHO syndrome and chronic recurrent multifocal osteomyelitis in typical patient groups. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Assmann%2C+Gunter%22">Assmann, Gunter</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Köhm%2C+Michaela%22">Köhm, Michaela</searchLink><relatesTo>2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Schuster%2C+Volker%22">Schuster, Volker</searchLink><relatesTo>3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Behrens%2C+Frank%22">Behrens, Frank</searchLink><relatesTo>2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Mössner%2C+Rotraut%22">Mössner, Rotraut</searchLink><relatesTo>4</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Magnolo%2C+Nina%22">Magnolo, Nina</searchLink><relatesTo>5</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Oji%2C+Vinzenz%22">Oji, Vinzenz</searchLink><relatesTo>5</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Burkhardt%2C+Harald%22">Burkhardt, Harald</searchLink><relatesTo>2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Hüffmeier%2C+Ulrike%22">Hüffmeier, Ulrike</searchLink><relatesTo>6</relatesTo> (AUTHOR)<i> ulrike.hueffmeier@uk-erlangen.de</i> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22BMC+Medical+Genetics%22">BMC Medical Genetics</searchLink>. 5/12/2020, Vol. 21 Issue 1, p1-7. 7p. |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=143169279 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1186/s12881-020-01037-7 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 7 StartPage: 1 Titles: – TitleFull: Genetic variants in FBLIM1 gene do not contribute to SAPHO syndrome and chronic recurrent multifocal osteomyelitis in typical patient groups. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Assmann, Gunter – PersonEntity: Name: NameFull: Köhm, Michaela – PersonEntity: Name: NameFull: Schuster, Volker – PersonEntity: Name: NameFull: Behrens, Frank – PersonEntity: Name: NameFull: Mössner, Rotraut – PersonEntity: Name: NameFull: Magnolo, Nina – PersonEntity: Name: NameFull: Oji, Vinzenz – PersonEntity: Name: NameFull: Burkhardt, Harald – PersonEntity: Name: NameFull: Hüffmeier, Ulrike IsPartOfRelationships: – BibEntity: Dates: – D: 12 M: 05 Text: 5/12/2020 Type: published Y: 2020 Identifiers: – Type: issn-print Value: 14712350 Numbering: – Type: volume Value: 21 – Type: issue Value: 1 Titles: – TitleFull: BMC Medical Genetics Type: main |
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