المؤلفون: Anzel Bahadır, Onur Öztürk, Ayfer Atalay, Erol Ömer Atalay

المصدر: Turkish Journal of Hematology, Vol 26, Iss 03, Pp 129-137 (2009)

مصطلحات موضوعية: Beta thalassemia, beta globin haplotypes, mutation, Diseases of the blood and blood-forming organs, RC633-647.5

وصف الملف: electronic resource

العلاقة: http://www.journalagent.com/z4/download_fulltext.asp?pdir=tjh&plng=eng&un=TJH-96168Test; https://doaj.org/toc/1300-7777Test; https://doaj.org/toc/1308-5263Test

الوصول الحر: https://doaj.org/article/a0cc4f3ac1d44525805ff85b0cf3e941Test

المؤلفون: Günfer Turgut, Sebahat Turgut, Osman Genc, Ayfer Atalay, Erol Ömer Atalay

المصدر: Acta Medica, Vol 47, Iss 2, Pp 133-136 (2004)

مصطلحات موضوعية: ACE I/D polymorphism, Athlete, Sedentary, Sports physiology, Physical performance, Medicine

وصف الملف: electronic resource

العلاقة: https://actamedica.lfhk.cuni.cz/47/2/0133Test/; https://doaj.org/toc/1211-4286Test; https://doaj.org/toc/1805-9694Test

الوصول الحر: https://doaj.org/article/3c0971b36ba346d8a553ec834863cfceTest

المؤلفون: Aylin Köseler, Hasan Koyuncu, Onur Öztürk, Anzel Bahadır, Sanem Demirtepe, Ayfer Atalay, Erol Ömer Atalay

المصدر: Turkish Journal of Hematology, Vol 27, Iss 02, Pp 120-122 (2010)

مصطلحات موضوعية: Hemoglobinopathy, abnormal hemoglobin, Hb Tunis, Diseases of the blood and blood-forming organs, RC633-647.5

وصف الملف: electronic resource

العلاقة: http://www.journalagent.com/z4/download_fulltext.asp?pdir=tjh&plng=eng&un=TJH-57070Test; https://doaj.org/toc/1300-7777Test; https://doaj.org/toc/1308-5263Test

الوصول الحر: https://doaj.org/article/c3a24d15689740dc9eecc347ca5c41bbTest

المؤلفون: Aylin Köseler, Ayfer Atalay, Erol Ömer Atalay

المصدر: Turkish Journal of Hematology, Vol 29, Iss 3, Pp 289-290 (2012)

مصطلحات موضوعية: hba2-yokoshima (delta 25(b7)gly >asp) and hb a2-yialousa (delta 27(b9)ala>ser) in turkey, Diseases of the blood and blood-forming organs, RC633-647.5

وصف الملف: electronic resource

العلاقة: https://jag.journalagent.com/z4/download_fulltext.asp?pdir=tjh&un=TJH-50470Test; https://doaj.org/toc/1308-5263Test

الوصول الحر: https://doaj.org/article/a6a2e61a33754398b8d5fdf9662777b5Test

المؤلفون: Hikmet Ergin Dülger, Mehmet Tokdemir, B. Erbağ, Erol Ömer Atalay, Mehmet Ziya Doymaz

المصدر: Adli Tıp Bülteni, Vol 2, Iss 1 (1997)

مصطلحات موضوعية: DNA parmak izi, DNA izolasyonu, adli tıp, Medicine (General), R5-920

وصف الملف: electronic resource

العلاقة: https://www.adlitipbulteni.com/atb/article/view/198Test; https://doaj.org/toc/1300-865XTest; https://doaj.org/toc/2149-4533Test

الوصول الحر: https://doaj.org/article/d8328824f3344444bec21de43eee9ccbTest

المؤلفون: Sanem Arıkan, Onur Öztürk, Şeniz Duygulu, Erol Ömer Atalay, Ayfer Atalay

مصطلحات موضوعية: Rheumatoid-Arthritis, Immunology, IL-17R, Population, SNP, Pathogenesis, Il17a, Behcet's disease, Interleukin-17 Gene Polymorphism, Asthma, IL-17, Susceptibility, 17a, Haplotype, Single-Nucleotide Polymorphisms

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7ae6e3ca4147f06152684112cc5c701Test
https://hdl.handle.net/11499/50379Test

المؤلفون: Erol Ömer Atalay, Ayfer Atalay, O. Öztürk, Şeniz Duygulu, Sanem Arikan

المصدر: Clinical and Experimental Dermatology. 46:1462-1470

مصطلحات موضوعية: Male, Risk, Chemokine CXCL5, Turkey, Single-nucleotide polymorphism, Dermatology, Behcet's disease, Disease, Biology, Polymorphism, Single Nucleotide, Receptors, Interleukin-8B, Receptors, Interleukin-8A, Pathogenesis, Polymorphism (computer science), Genotype, medicine, Humans, Genetic Predisposition to Disease, Il-8 Gene, Genotyping, Genetics, Sclerosis, Behcet Syndrome, Population-Genetics, Haplotype, Conversion, hemic and immune systems, medicine.disease, Haplotypes, Chemokine, Female

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c282c8dbf754e7fbd1a21f88eb587228Test
https://doi.org/10.1111/ced.14766Test

المؤلفون: Sanem Arikan, Onur Ozturk, Ayfer Atalay, Erol Ömer Atalay

المصدر: Molecular Genetics & Genomic Medicine

مصطلحات موضوعية: 0301 basic medicine, haplotype, Hemoglobins, Abnormal, Population, ß-globin gene cluster, population group, hemoglobin variant, Biology, phylogeny, 03 medical and health sciences, hemoglobin D Punjab, 0302 clinical medicine, Population Groups, Gene cluster, phylogenetic network analysis, Genetics, Hb D‐Los Angeles, Hb D-Los Angeles, Humans, genetics, human, education, Molecular Biology, Genetics (clinical), time estimate, education.field_of_study, Models, Genetic, Haplotype, Original Articles, Phylogenetic network, biological model, Restriction site, 030104 developmental biology, Haplotypes, Mutation, Mutation (genetic algorithm), β-globin gene cluster, Original Article, Gene pool, β‐globin gene cluster, Restriction fragment length polymorphism, 030215 immunology

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1e417a29aafeeb51a3e54cbff9f693dTest
https://doi.org/10.1002/mgg3.499Test

المؤلفون: Aylin Köseler, Anzel Bahad›r, Hasan Koyuncu, Ayfer Atalay, Erol Ömer Atalay

المساهمون: The Pennsylvania State University CiteSeerX Archives

المصدر: http://www.journalagent.com/tjh/pdfs/TJH_25_1_51_53.pdfTest.

وصف الملف: application/pdf

العلاقة: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.1069.7926Test; http://www.journalagent.com/tjh/pdfs/TJH_25_1_51_53.pdfTest

الإتاحة: http://www.journalagent.com/tjh/pdfs/TJH_25_1_51_53.pdfTest

المؤلفون: Hülya Halis, Aylin Köseler, Erol Ömer Atalay, Hacer Ergin

المصدر: The Journal of Maternal-Fetal & Neonatal Medicine. 30:2658-2664

مصطلحات موضوعية: Male, Turkey, genotype, polymerase chain reaction, neonatal hyperbilirubinemia, glucuronosyltransferase 1A1, Gene mutation, glucuronosyltransferase, Gastroenterology, blood group ABO system, immunology, chemistry.chemical_compound, Exon, 0302 clinical medicine, newborn, Pregnancy, Genotype, genetic polymorphism, guanine, genetics, exon, gene mutation, 030212 general & internal medicine, Glucuronosyltransferase, gestational age, Promoter Regions, Genetic, Exon-1 mutation, Hyperbilirubinemia, bilirubin blood level, blood group incompatibility, Promoter polymorphism, Obstetrics and Gynecology, Exons, Jaundice, Jaundice, Neonatal, homozygote, female, priority journal, Blood Group Incompatibility, disease severity, Female, bilirubin, Hyperbilirubinemia, Neonatal, medicine.symptom, congenital, hereditary, and neonatal diseases and abnormalities, medicine.medical_specialty, Bilirubin, education, Gestational Age, gene sequence, gene frequency, Article, ABO Blood-Group System, 03 medical and health sciences, promoter region, blood, 030225 pediatrics, Internal medicine, ABO blood group system, medicine, Humans, controlled study, Genetic Predisposition to Disease, human, adenine, Allele frequency, Polymorphism, Genetic, business.industry, UGT1A1 enzyme, Infant, Newborn, Case-control study, DNA, case control study, heterozygote, major clinical study, Molecular biology, blood group ABO incompatibility, gene function, chemistry, DNA polymorphism, Case-Control Studies, Mutation, Pediatrics, Perinatology and Child Health, Turk (people), newborn jaundice, UGT1A1 gene, business, genetic predisposition

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f23d9fe82ba3b08b3f70309eaec517ccTest
https://doi.org/10.1080/14767058.2016.1261105Test