Genetic variants in FBLIM1 gene do not contribute to SAPHO syndrome and chronic recurrent multifocal osteomyelitis in typical patient groups:
Gespeichert in:
| Beteiligte Personen: | , , , , , , , , |
|---|---|
| Format: | Elektronisch E-Book |
| Sprache: | Englisch |
| Veröffentlicht: |
Erlangen ; Nürnberg
Friedrich-Alexander-Universität Erlangen-Nürnberg
2020
|
| Schlagwörter: | |
| Links: | https://doi.org/10.1186/s12881-020-01037-7 https://nbn-resolving.org/urn:nbn:de:bvb:29-opus4-143648 https://open.fau.de/handle/openfau/14364 |
| Umfang: | 1 Online-Ressource |
| DOI: | 10.1186/s12881-020-01037-7 |
Internformat
MARC
| LEADER | 00000nam a2200000zc 4500 | ||
|---|---|---|---|
| 001 | BV046886552 | ||
| 003 | DE-604 | ||
| 005 | 00000000000000.0 | ||
| 007 | cr|uuu---uuuuu | ||
| 008 | 200907s2020 gw o|||| 00||| eng d | ||
| 024 | 7 | |a 10.1186/s12881-020-01037-7 |2 doi | |
| 024 | 7 | |a urn:nbn:de:bvb:29-opus4-143648 |2 urn | |
| 035 | |a (OCoLC)1197701701 | ||
| 035 | |a (DE-599)BVBBV046886552 | ||
| 040 | |a DE-604 |b ger |e rda | ||
| 041 | 0 | |a eng | |
| 044 | |a gw |c XA-DE | ||
| 049 | |a DE-29 | ||
| 084 | |a 610 |2 sdnb | ||
| 084 | |a 616.042 |2 sdnb | ||
| 100 | 1 | |a Assmann, Gunter |e Verfasser |4 aut | |
| 245 | 1 | 0 | |a Genetic variants in FBLIM1 gene do not contribute to SAPHO syndrome and chronic recurrent multifocal osteomyelitis in typical patient groups |c Gunter Assmann, Michaela Köhm, Volker Schuster, Frank Behrens, Rotraut Mössner, Nina Magnolo, Vinzenz Oji, Harald Burkhardt, Ulrike Hüffmeier |
| 264 | 1 | |a Erlangen ; Nürnberg |b Friedrich-Alexander-Universität Erlangen-Nürnberg |c 2020 | |
| 300 | |a 1 Online-Ressource | ||
| 336 | |b txt |2 rdacontent | ||
| 337 | |b c |2 rdamedia | ||
| 338 | |b cr |2 rdacarrier | ||
| 650 | 0 | |a Human genetics. | |
| 650 | 0 | |a Medical genetics. | |
| 650 | 0 | |a Cytogenetics. | |
| 653 | |a Human Genetics. | ||
| 653 | |a Cytogenetics. | ||
| 653 | |a Gene Function. | ||
| 700 | 1 | |a Köhm, Michaela |e Verfasser |4 aut | |
| 700 | 1 | |a Schuster, Volker |e Verfasser |4 aut | |
| 700 | 1 | |a Behrens, Frank |e Verfasser |4 aut | |
| 700 | 1 | |a Mössner, Rotraut |e Verfasser |4 aut | |
| 700 | 1 | |a Magnolo, Nina |e Verfasser |4 aut | |
| 700 | 1 | |a Oji, Vinzenz |e Verfasser |4 aut | |
| 700 | 1 | |a Burkhardt, Harald |e Verfasser |4 aut | |
| 700 | 1 | |a Hüffmeier, Ulrike |e Verfasser |4 aut | |
| 787 | 0 | 8 | |i Sonderdruck aus |t BMC Medical Genetics |g Vol. 21 (2020) |o 10.1186/s12881-020-01037-7 |
| 856 | 4 | 0 | |u https://doi.org/10.1186/s12881-020-01037-7 |x Resolving-System |z kostenfrei |3 Volltext |
| 856 | 4 | 0 | |u https://nbn-resolving.org/urn:nbn:de:bvb:29-opus4-143648 |x Resolving-System |z kostenfrei |3 Volltext |
| 856 | 4 | 0 | |u https://open.fau.de/handle/openfau/14364 |x Verlag |z kostenfrei |3 Volltext |
| 912 | |a ebook | ||
| 943 | 1 | |a oai:aleph.bib-bvb.de:BVB01-032296455 | |
Datensatz im Suchindex
| _version_ | 1818987255268638720 |
|---|---|
| any_adam_object | |
| author | Assmann, Gunter Köhm, Michaela Schuster, Volker Behrens, Frank Mössner, Rotraut Magnolo, Nina Oji, Vinzenz Burkhardt, Harald Hüffmeier, Ulrike |
| author_facet | Assmann, Gunter Köhm, Michaela Schuster, Volker Behrens, Frank Mössner, Rotraut Magnolo, Nina Oji, Vinzenz Burkhardt, Harald Hüffmeier, Ulrike |
| author_role | aut aut aut aut aut aut aut aut aut |
| author_sort | Assmann, Gunter |
| author_variant | g a ga m k mk v s vs f b fb r m rm n m nm v o vo h b hb u h uh |
| building | Verbundindex |
| bvnumber | BV046886552 |
| collection | ebook |
| ctrlnum | (OCoLC)1197701701 (DE-599)BVBBV046886552 |
| discipline | Medizin |
| doi_str_mv | 10.1186/s12881-020-01037-7 |
| format | Electronic eBook |
| fullrecord | <?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>02128nam a2200529zc 4500</leader><controlfield tag="001">BV046886552</controlfield><controlfield tag="003">DE-604</controlfield><controlfield tag="005">00000000000000.0</controlfield><controlfield tag="007">cr|uuu---uuuuu</controlfield><controlfield tag="008">200907s2020 gw o|||| 00||| eng d</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1186/s12881-020-01037-7</subfield><subfield code="2">doi</subfield></datafield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">urn:nbn:de:bvb:29-opus4-143648</subfield><subfield code="2">urn</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(OCoLC)1197701701</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-599)BVBBV046886552</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-604</subfield><subfield code="b">ger</subfield><subfield code="e">rda</subfield></datafield><datafield tag="041" ind1="0" ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="044" ind1=" " ind2=" "><subfield code="a">gw</subfield><subfield code="c">XA-DE</subfield></datafield><datafield tag="049" ind1=" " ind2=" "><subfield code="a">DE-29</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">610</subfield><subfield code="2">sdnb</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">616.042</subfield><subfield code="2">sdnb</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Assmann, Gunter</subfield><subfield code="e">Verfasser</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Genetic variants in FBLIM1 gene do not contribute to SAPHO syndrome and chronic recurrent multifocal osteomyelitis in typical patient groups</subfield><subfield code="c">Gunter Assmann, Michaela Köhm, Volker Schuster, Frank Behrens, Rotraut Mössner, Nina Magnolo, Vinzenz Oji, Harald Burkhardt, Ulrike Hüffmeier</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="a">Erlangen ; Nürnberg</subfield><subfield code="b">Friedrich-Alexander-Universität Erlangen-Nürnberg</subfield><subfield code="c">2020</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">1 Online-Ressource</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="650" ind1=" " ind2="0"><subfield code="a">Human genetics.</subfield></datafield><datafield tag="650" ind1=" " ind2="0"><subfield code="a">Medical genetics.</subfield></datafield><datafield tag="650" ind1=" " ind2="0"><subfield code="a">Cytogenetics.</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Human Genetics.</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Cytogenetics.</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Gene Function.</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Köhm, Michaela</subfield><subfield code="e">Verfasser</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Schuster, Volker</subfield><subfield code="e">Verfasser</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Behrens, Frank</subfield><subfield code="e">Verfasser</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Mössner, Rotraut</subfield><subfield code="e">Verfasser</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Magnolo, Nina</subfield><subfield code="e">Verfasser</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Oji, Vinzenz</subfield><subfield code="e">Verfasser</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Burkhardt, Harald</subfield><subfield code="e">Verfasser</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Hüffmeier, Ulrike</subfield><subfield code="e">Verfasser</subfield><subfield code="4">aut</subfield></datafield><datafield tag="787" ind1="0" ind2="8"><subfield code="i">Sonderdruck aus</subfield><subfield code="t">BMC Medical Genetics</subfield><subfield code="g">Vol. 21 (2020)</subfield><subfield code="o">10.1186/s12881-020-01037-7</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">https://doi.org/10.1186/s12881-020-01037-7</subfield><subfield code="x">Resolving-System</subfield><subfield code="z">kostenfrei</subfield><subfield code="3">Volltext</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">https://nbn-resolving.org/urn:nbn:de:bvb:29-opus4-143648</subfield><subfield code="x">Resolving-System</subfield><subfield code="z">kostenfrei</subfield><subfield code="3">Volltext</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">https://open.fau.de/handle/openfau/14364</subfield><subfield code="x">Verlag</subfield><subfield code="z">kostenfrei</subfield><subfield code="3">Volltext</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">ebook</subfield></datafield><datafield tag="943" ind1="1" ind2=" "><subfield code="a">oai:aleph.bib-bvb.de:BVB01-032296455</subfield></datafield></record></collection> |
| id | DE-604.BV046886552 |
| illustrated | Not Illustrated |
| indexdate | 2024-12-20T19:03:47Z |
| institution | BVB |
| language | English |
| oai_aleph_id | oai:aleph.bib-bvb.de:BVB01-032296455 |
| oclc_num | 1197701701 |
| open_access_boolean | 1 |
| owner | DE-29 |
| owner_facet | DE-29 |
| physical | 1 Online-Ressource |
| psigel | ebook |
| publishDate | 2020 |
| publishDateSearch | 2020 |
| publishDateSort | 2020 |
| publisher | Friedrich-Alexander-Universität Erlangen-Nürnberg |
| record_format | marc |
| spelling | Assmann, Gunter Verfasser aut Genetic variants in FBLIM1 gene do not contribute to SAPHO syndrome and chronic recurrent multifocal osteomyelitis in typical patient groups Gunter Assmann, Michaela Köhm, Volker Schuster, Frank Behrens, Rotraut Mössner, Nina Magnolo, Vinzenz Oji, Harald Burkhardt, Ulrike Hüffmeier Erlangen ; Nürnberg Friedrich-Alexander-Universität Erlangen-Nürnberg 2020 1 Online-Ressource txt rdacontent c rdamedia cr rdacarrier Human genetics. Medical genetics. Cytogenetics. Human Genetics. Gene Function. Köhm, Michaela Verfasser aut Schuster, Volker Verfasser aut Behrens, Frank Verfasser aut Mössner, Rotraut Verfasser aut Magnolo, Nina Verfasser aut Oji, Vinzenz Verfasser aut Burkhardt, Harald Verfasser aut Hüffmeier, Ulrike Verfasser aut Sonderdruck aus BMC Medical Genetics Vol. 21 (2020) 10.1186/s12881-020-01037-7 https://doi.org/10.1186/s12881-020-01037-7 Resolving-System kostenfrei Volltext https://nbn-resolving.org/urn:nbn:de:bvb:29-opus4-143648 Resolving-System kostenfrei Volltext https://open.fau.de/handle/openfau/14364 Verlag kostenfrei Volltext |
| spellingShingle | Assmann, Gunter Köhm, Michaela Schuster, Volker Behrens, Frank Mössner, Rotraut Magnolo, Nina Oji, Vinzenz Burkhardt, Harald Hüffmeier, Ulrike Genetic variants in FBLIM1 gene do not contribute to SAPHO syndrome and chronic recurrent multifocal osteomyelitis in typical patient groups Human genetics. Medical genetics. Cytogenetics. |
| title | Genetic variants in FBLIM1 gene do not contribute to SAPHO syndrome and chronic recurrent multifocal osteomyelitis in typical patient groups |
| title_auth | Genetic variants in FBLIM1 gene do not contribute to SAPHO syndrome and chronic recurrent multifocal osteomyelitis in typical patient groups |
| title_exact_search | Genetic variants in FBLIM1 gene do not contribute to SAPHO syndrome and chronic recurrent multifocal osteomyelitis in typical patient groups |
| title_full | Genetic variants in FBLIM1 gene do not contribute to SAPHO syndrome and chronic recurrent multifocal osteomyelitis in typical patient groups Gunter Assmann, Michaela Köhm, Volker Schuster, Frank Behrens, Rotraut Mössner, Nina Magnolo, Vinzenz Oji, Harald Burkhardt, Ulrike Hüffmeier |
| title_fullStr | Genetic variants in FBLIM1 gene do not contribute to SAPHO syndrome and chronic recurrent multifocal osteomyelitis in typical patient groups Gunter Assmann, Michaela Köhm, Volker Schuster, Frank Behrens, Rotraut Mössner, Nina Magnolo, Vinzenz Oji, Harald Burkhardt, Ulrike Hüffmeier |
| title_full_unstemmed | Genetic variants in FBLIM1 gene do not contribute to SAPHO syndrome and chronic recurrent multifocal osteomyelitis in typical patient groups Gunter Assmann, Michaela Köhm, Volker Schuster, Frank Behrens, Rotraut Mössner, Nina Magnolo, Vinzenz Oji, Harald Burkhardt, Ulrike Hüffmeier |
| title_short | Genetic variants in FBLIM1 gene do not contribute to SAPHO syndrome and chronic recurrent multifocal osteomyelitis in typical patient groups |
| title_sort | genetic variants in fblim1 gene do not contribute to sapho syndrome and chronic recurrent multifocal osteomyelitis in typical patient groups |
| topic | Human genetics. Medical genetics. Cytogenetics. |
| topic_facet | Human genetics. Medical genetics. Cytogenetics. |
| url | https://doi.org/10.1186/s12881-020-01037-7 https://nbn-resolving.org/urn:nbn:de:bvb:29-opus4-143648 https://open.fau.de/handle/openfau/14364 |
| work_keys_str_mv | AT assmanngunter geneticvariantsinfblim1genedonotcontributetosaphosyndromeandchronicrecurrentmultifocalosteomyelitisintypicalpatientgroups AT kohmmichaela geneticvariantsinfblim1genedonotcontributetosaphosyndromeandchronicrecurrentmultifocalosteomyelitisintypicalpatientgroups AT schustervolker geneticvariantsinfblim1genedonotcontributetosaphosyndromeandchronicrecurrentmultifocalosteomyelitisintypicalpatientgroups AT behrensfrank geneticvariantsinfblim1genedonotcontributetosaphosyndromeandchronicrecurrentmultifocalosteomyelitisintypicalpatientgroups AT mossnerrotraut geneticvariantsinfblim1genedonotcontributetosaphosyndromeandchronicrecurrentmultifocalosteomyelitisintypicalpatientgroups AT magnolonina geneticvariantsinfblim1genedonotcontributetosaphosyndromeandchronicrecurrentmultifocalosteomyelitisintypicalpatientgroups AT ojivinzenz geneticvariantsinfblim1genedonotcontributetosaphosyndromeandchronicrecurrentmultifocalosteomyelitisintypicalpatientgroups AT burkhardtharald geneticvariantsinfblim1genedonotcontributetosaphosyndromeandchronicrecurrentmultifocalosteomyelitisintypicalpatientgroups AT huffmeierulrike geneticvariantsinfblim1genedonotcontributetosaphosyndromeandchronicrecurrentmultifocalosteomyelitisintypicalpatientgroups |