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https://hdl.handle.net/11499/4144
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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Atalay, Ayfer. | - |
dc.contributor.author | Koyuncu, H. | - |
dc.contributor.author | Köseler, Aylin. | - |
dc.contributor.author | Ozkan, A. | - |
dc.contributor.author | Atalay, E.Ö. | - |
dc.date.accessioned | 2019-08-16T11:32:23Z | - |
dc.date.available | 2019-08-16T11:32:23Z | - |
dc.date.issued | 2007 | - |
dc.identifier.issn | 0363-0269 | - |
dc.identifier.uri | https://hdl.handle.net/11499/4144 | - |
dc.identifier.uri | https://doi.org/10.1080/03630260701590335 | - |
dc.description.abstract | Hb Beograd [ß121(GH4)Glu›Val, GAA›GTA] is a rare variant first reported in Yugoslavia and then in Turkey, Australia and New Zealand. We report two further unrelated cases from Turkey. The importance of identifying Hb Beograd at the molecular level, especially in regions where Hb D-Los Angeles [ß121(GH4)Glu›Gln, GAA›CAA] is prevalent, is emphasized. Copyright © Informa Healthcare USA, Inc. | en_US |
dc.language.iso | en | en_US |
dc.relation.ispartof | Hemoglobin | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Hb Beograd | en_US |
dc.subject | Premarital screening | en_US |
dc.subject | glutamic acid | en_US |
dc.subject | glutamine | en_US |
dc.subject | hemoglobin beograd | en_US |
dc.subject | hemoglobin d punjab | en_US |
dc.subject | hemoglobin variant | en_US |
dc.subject | unclassified drug | en_US |
dc.subject | valine | en_US |
dc.subject | amino acid substitution | en_US |
dc.subject | article | en_US |
dc.subject | Australia | en_US |
dc.subject | case report | en_US |
dc.subject | DNA sequence | en_US |
dc.subject | electrophoresis | en_US |
dc.subject | female | en_US |
dc.subject | gene cluster | en_US |
dc.subject | gene mutation | en_US |
dc.subject | genetic counseling | en_US |
dc.subject | genetic screening | en_US |
dc.subject | genetic variability | en_US |
dc.subject | haplotype | en_US |
dc.subject | high performance liquid chromatography | en_US |
dc.subject | human | en_US |
dc.subject | male | en_US |
dc.subject | New Zealand | en_US |
dc.subject | Turkey (republic) | en_US |
dc.subject | Yugoslavia | en_US |
dc.subject | beta thalassemia | en_US |
dc.subject | chemistry | en_US |
dc.subject | ethnology | en_US |
dc.subject | genetics | en_US |
dc.subject | point mutation | en_US |
dc.subject | Amino Acid Substitution | en_US |
dc.subject | beta-Thalassemia | en_US |
dc.subject | Female | en_US |
dc.subject | Hemoglobins, Abnormal | en_US |
dc.subject | Humans | en_US |
dc.subject | Male | en_US |
dc.subject | Point Mutation | en_US |
dc.subject | Turkey | en_US |
dc.title | Hb Beograd [ß121(GH4)Glu›Val, GAA›GTA] in the Turkish population | en_US |
dc.type | Article | en_US |
dc.identifier.volume | 31 | en_US |
dc.identifier.issue | 4 | en_US |
dc.identifier.startpage | 491 | - |
dc.identifier.startpage | 491 | en_US |
dc.identifier.endpage | 493 | en_US |
dc.identifier.doi | 10.1080/03630260701590335 | - |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.identifier.pmid | 17994384 | en_US |
dc.identifier.scopus | 2-s2.0-36249026342 | en_US |
dc.identifier.wos | WOS:000250921600012 | en_US |
dc.identifier.scopusquality | Q3 | - |
dc.owner | Pamukkale University | - |
item.fulltext | No Fulltext | - |
item.grantfulltext | none | - |
item.languageiso639-1 | en | - |
item.openairetype | Article | - |
item.cerifentitytype | Publications | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
crisitem.author.dept | 14.03. Basic Medical Sciences | - |
crisitem.author.dept | 14.03. Basic Medical Sciences | - |
crisitem.author.dept | 14.03. Basic Medical Sciences | - |
Appears in Collections: | PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection Tıp Fakültesi Koleksiyonu WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection |
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