date: 2015-07-27T21:58:47Z pdf:PDFVersion: 1.7 pdf:docinfo:title: FGFR2 mutation in a patient without typical features of Pfeiffer syndrome - The emerging role of combined NGS and phenotype based strategies xmp:CreatorTool: Elsevier access_permission:can_print_degraded: true subject: European Journal of Medical Genetics, 58 (2015) 376-380. doi:10.1016/j.ejmg.2015.05.007 dc:format: application/pdf; version=1.7 pdf:docinfo:custom:robots: noindex pdf:docinfo:creator_tool: Elsevier access_permission:fill_in_form: true pdf:docinfo:custom:CreationDate--Text: 28th July 2015 pdf:encrypted: false dc:title: FGFR2 mutation in a patient without typical features of Pfeiffer syndrome - The emerging role of combined NGS and phenotype based strategies modified: 2015-07-27T21:58:47Z cp:subject: European Journal of Medical Genetics, 58 (2015) 376-380. doi:10.1016/j.ejmg.2015.05.007 robots: noindex pdf:docinfo:custom:CrossMarkDomains[1]: sciencedirect.com pdf:docinfo:subject: European Journal of Medical Genetics, 58 (2015) 376-380. doi:10.1016/j.ejmg.2015.05.007 pdf:docinfo:creator: Ricarda Flöttmann meta:author: Alexej Knaus pdf:docinfo:custom:CrossmarkMajorVersionDate: 2010-04-23 access_permission:extract_for_accessibility: true pdf:docinfo:custom:CrossMarkDomains[2]: elsevier.com ElsevierWebPDFSpecifications: 6.4 pdf:docinfo:custom:doi: 10.1016/j.ejmg.2015.05.007 pdf:docinfo:custom:CrossmarkDomainExclusive: true Author: Alexej Knaus producer: Acrobat Distiller 8.1.0 (Windows) CrossmarkDomainExclusive: true pdf:docinfo:producer: Acrobat Distiller 8.1.0 (Windows) CreationDate--Text: 28th July 2015 doi: 10.1016/j.ejmg.2015.05.007 pdf:unmappedUnicodeCharsPerPage: 2 dc:description: European Journal of Medical Genetics, 58 (2015) 376-380. doi:10.1016/j.ejmg.2015.05.007 access_permission:modify_annotations: true dc:creator: Alexej Knaus description: European Journal of Medical Genetics, 58 (2015) 376-380. doi:10.1016/j.ejmg.2015.05.007 Last-Modified: 2015-07-27T21:58:47Z dcterms:modified: 2015-07-27T21:58:47Z title: FGFR2 mutation in a patient without typical features of Pfeiffer syndrome - The emerging role of combined NGS and phenotype based strategies xmpMM:DocumentID: uuid:22f90538-c060-40df-8447-3af1949ebb47 Last-Save-Date: 2015-07-27T21:58:47Z CrossMarkDomains[1]: sciencedirect.com pdf:docinfo:modified: 2015-07-27T21:58:47Z meta:save-date: 2015-07-27T21:58:47Z Content-Type: application/pdf X-Parsed-By: org.apache.tika.parser.DefaultParser creator: Alexej Knaus pdf:docinfo:custom:ElsevierWebPDFSpecifications: 6.4 access_permission:assemble_document: true xmpTPg:NPages: 5 pdf:charsPerPage: 3726 access_permission:extract_content: true access_permission:can_print: true CrossMarkDomains[2]: elsevier.com access_permission:can_modify: true CrossmarkMajorVersionDate: 2010-04-23