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| http://purl.uniprot.org/citations/30025477 | http://www.w3.org/2000/01/rdf-schema#comment | "Hb Adana (HBA2: c.179G>A) is found worldwide but is extremely rare and carriers are asymptomatic, with red cell indices similar to α+-thalassemia (α+-thal) carriers. First line screening tests are unable to detect the unstable hemoglobin (Hb). Coinheritance with the α-thal (-α3.7) deletion is herein presented and the challenges involving genetic counseling of couples carrying the mutations are discussed."xsd:string |
| http://purl.uniprot.org/citations/30025477 | http://purl.org/dc/terms/identifier | "doi:10.1080/03630269.2018.1466711"xsd:string |
| http://purl.uniprot.org/citations/30025477 | http://purl.uniprot.org/core/author | "Vyzantiadis T.A."xsd:string |
| http://purl.uniprot.org/citations/30025477 | http://purl.uniprot.org/core/author | "Theodoridou S."xsd:string |
| http://purl.uniprot.org/citations/30025477 | http://purl.uniprot.org/core/author | "Yfanti E."xsd:string |
| http://purl.uniprot.org/citations/30025477 | http://purl.uniprot.org/core/author | "Economou M."xsd:string |
| http://purl.uniprot.org/citations/30025477 | http://purl.uniprot.org/core/author | "Theodoridis T."xsd:string |
| http://purl.uniprot.org/citations/30025477 | http://purl.uniprot.org/core/author | "Teli A."xsd:string |
| http://purl.uniprot.org/citations/30025477 | http://purl.uniprot.org/core/date | "2018"xsd:gYear |
| http://purl.uniprot.org/citations/30025477 | http://purl.uniprot.org/core/name | "Hemoglobin"xsd:string |
| http://purl.uniprot.org/citations/30025477 | http://purl.uniprot.org/core/pages | "129-131"xsd:string |
| http://purl.uniprot.org/citations/30025477 | http://purl.uniprot.org/core/title | "Compound Heterozygosity for Hb Adana (HBA2: c.179G>A) and the -alphapisup>3.7pi/sup>/alphaalpha Thalassemia Deletion in Greece: Clinical Phenotype and Genetic Counseling."xsd:string |
| http://purl.uniprot.org/citations/30025477 | http://purl.uniprot.org/core/volume | "42"xsd:string |
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