Authors' reply
dc.contributor.author | Constantinou-Deltas, Constantinos D. | en |
dc.contributor.author | Voskarides, Konstantinos | en |
dc.creator | Constantinou-Deltas, Constantinos D. | en |
dc.creator | Voskarides, Konstantinos | en |
dc.date.accessioned | 2019-11-04T12:50:29Z | |
dc.date.available | 2019-11-04T12:50:29Z | |
dc.date.issued | 2010 | |
dc.identifier.issn | 1525-1578 | |
dc.identifier.uri | http://gnosis.library.ucy.ac.cy/handle/7/53037 | |
dc.source | Journal of Molecular Diagnostics | en |
dc.source.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-77649165924&doi=10.2353%2fjmoldx.2010.090193&partnerID=40&md5=bd1616e89851f7bb168627da69042d4d | |
dc.subject | human | en |
dc.subject | DNA polymorphism | en |
dc.subject | letter | en |
dc.subject | molecular genetics | en |
dc.subject | laboratory diagnosis | en |
dc.subject | diagnostic accuracy | en |
dc.subject | gene mutation | en |
dc.subject | gene deletion | en |
dc.subject | gene location | en |
dc.subject | sensitivity and specificity | en |
dc.subject | diagnostic procedure | en |
dc.subject | genetic variability | en |
dc.subject | DNA sequence | en |
dc.subject | amino acid substitution | en |
dc.subject | Alport syndrome | en |
dc.subject | amplicon | en |
dc.subject | monogenic disorder | en |
dc.subject | nephronophthisis | en |
dc.title | Authors' reply | en |
dc.type | info:eu-repo/semantics/article | |
dc.identifier.doi | 10.2353/jmoldx.2010.090193 | |
dc.description.volume | 12 | |
dc.description.startingpage | 265 | |
dc.description.endingpage | 266 | |
dc.author.faculty | Σχολή Θετικών και Εφαρμοσμένων Επιστημών / Faculty of Pure and Applied Sciences | |
dc.author.department | Τμήμα Βιολογικών Επιστημών / Department of Biological Sciences | |
dc.type.uhtype | Article | en |
dc.source.abbreviation | J.Mol.Diagn. | en |
dc.contributor.orcid | Constantinou-Deltas, Constantinos D. [0000-0001-5549-9169] | |
dc.gnosis.orcid | 0000-0001-5549-9169 |
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