Publication: Next Generation Sequencing (NGS) panel revealed new candidate genes and variants in 25 Hypertrophic Cardiomyopathy patients
| dc.conference.date | JUN 16-19, 2018 | |
| dc.conference.location | Milan, Italy | |
| dc.conference.organizer | 51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG) | |
| dc.contributor.coauthor | Turkgenc, B. | |
| dc.contributor.coauthor | Temel, S. G. | |
| dc.contributor.coauthor | Uysal, F. | |
| dc.contributor.coauthor | Atik, S. Ugan | |
| dc.contributor.coauthor | Oztunc, F. | |
| dc.contributor.coauthor | Sulu, A. | |
| dc.contributor.coauthor | Ekici, F. | |
| dc.contributor.coauthor | Ayabakan, C. | |
| dc.contributor.coauthor | Odemis, E. | |
| dc.contributor.coauthor | Saygili, A. | |
| dc.contributor.coauthor | Koka, A. | |
| dc.contributor.coauthor | Akinci, I. Ozkan | |
| dc.contributor.coauthor | Alanay, Y. | |
| dc.contributor.coauthor | Ozer, A. | |
| dc.contributor.coauthor | Yakicier, M. C. | |
| dc.contributor.department | School of Medicine | |
| dc.contributor.facultymember | No | |
| dc.contributor.kuauthor | Çeliker, Alpay | |
| dc.contributor.schoolcollegeinstitute | SCHOOL OF MEDICINE | |
| dc.date.accessioned | 2024-11-09T22:59:40Z | |
| dc.date.issued | 2019 | |
| dc.description.fulltext | No | |
| dc.description.harvestedfrom | Manual | |
| dc.description.indexedby | WOS | |
| dc.description.openaccess | NO | |
| dc.description.peerreviewstatus | N/A | |
| dc.description.publisherscope | International | |
| dc.description.readpublish | N/A | |
| dc.description.sponsoredbyTubitakEu | N/A | |
| dc.description.sponsorship | SANTEZ Grant | |
| dc.description.studentonlypublication | No | |
| dc.description.studentpublication | No | |
| dc.description.version | N/A | |
| dc.identifier.WoSQuartile | Q1 | |
| dc.identifier.eissn | 1476-5438 | |
| dc.identifier.embargo | N/A | |
| dc.identifier.endpage | 150 | |
| dc.identifier.grantno | 0253, STZ.2013-2 | |
| dc.identifier.issn | 1018-4813 | |
| dc.identifier.issue | Supplement 1 | |
| dc.identifier.startpage | 150 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.14288/7934 | |
| dc.identifier.volume | 27 | |
| dc.identifier.wos | 000489313101093 | |
| dc.keywords | Hypertrophic cardiomyopathy | |
| dc.keywords | Next generation sequencing | |
| dc.keywords | Genes | |
| dc.language.iso | eng | |
| dc.publisher | Springer Nature | |
| dc.relation.affiliation | Koç University | |
| dc.relation.collection | Koç University Institutional Repository | |
| dc.relation.ispartof | European Journal of Human Genetics | |
| dc.relation.openaccess | N/A | |
| dc.rights | N/A | |
| dc.subject | Biochemistry | |
| dc.subject | Molecular biology | |
| dc.subject | Genetics | |
| dc.subject | Heredity | |
| dc.title | Next Generation Sequencing (NGS) panel revealed new candidate genes and variants in 25 Hypertrophic Cardiomyopathy patients | |
| dc.type | Meeting Abstract | |
| dspace.entity.type | Publication | |
| local.contributor.kuauthor | Çeliker, Alpay | |
| relation.isOrgUnitOfPublication | d02929e1-2a70-44f0-ae17-7819f587bedd | |
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