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المؤلفون: Reyhan Gündüz, Rezan Buğday, Ahmet Yalinkaya, Diclehan Oral, Senem Yaman Tunç, Selahaddin Tekes
المصدر: Perinatal Journal, Vol 29, Iss 1, Pp 63-70 (2021)
مصطلحات موضوعية: medicine.medical_specialty, medicine.diagnostic_test, Obstetrics, business.industry, Gynecology and obstetrics, General Medicine, Pediatrics, RJ1-570, Second trimester, RG1-991, medicine, Amniocentesis, Center (algebra and category theory), business
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::261390d994e7d99c0c05e6f1c13d7ea2
https://doi.org/10.2399/prn.21.0291010 -
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المؤلفون: Diclehan Oral, Veysiye Hülya Üzel, Mehmet Akif Çürük, Selda Şimşek, Murat Söker, Selahaddin Tekes
المساهمون: Dicle Üniversitesi, Tıp Fakültesi, Temel Tıp Bilimleri Bölümü, Tıbbi Biyoloji Ana Bilim Dalı, Tekeş, Selahaddin, Oral, Diclehan, Söker, Murat, Uzel, Veysiye Hülya
مصطلحات موضوعية: Turkey, HBB:c.208G > A, Clinical Biochemistry, Trait, Prenatal-Diagnosis, Biology, Güneydoğu Anadolu Bölgesi, Biochemistry, Beta-thalassemia, beta-thalassemia, β-talasemi, Disease, Variant, Molecular Biology, Genetics, HBB:c.34G > A, c.208G > A [HBB], Biochemistry (medical), c.208G>A [HBB], Sickle-Cell-Anemia, c.34G>A [HBB], Hemoglobinopathies, Thalassemia, Beta globin gene, southeastern Anatolia region, c.34G > A [HBB], Southeastern Anatolia region
وصف الملف: application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9fdeb65ece4400a20264343b1d1b73b1
https://doi.org/10.1515/tjb-2020-0546 -
3The distribution of MEFV mutations in children FMF patients: Single center study in southeast Turkey
المؤلفون: Mahir BİNİCİ, Selahaddin TEKEŞ, Mahmut BALKAN, Diclehan ORAL, İlyas YÜCEL, Şaban TUNÇ
المساهمون: Dicle Üniversitesi, Tıp Fakültesi, Temel Tıp Bilimleri Bölümü, Tıbbi Biyoloji Ana Bilim Dalı, Binici, Mahir, Tekeş, Selahaddin, Balkan, Mahmut, Oral, Diclehan, Yücel, İlyas, Tunç, Şaban
المصدر: Volume: 49, Issue: 2 361-366
Dicle Tıp Dergisiمصطلحات موضوعية: Mutasyon, Autoinflammatory disease, Otoinflamatuar hastalık, Health Care Sciences and Services, MEFV gene, Familial mediterranean fever, Otoinflamatuar hastalık,Ailesel Akdeniz Ateşi,MEFV geni,Mutasyon, Ailesel akdeniz ateşi, MEFV geni, Sağlık Bilimleri ve Hizmetleri, Mutations
وصف الملف: application/pdf
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المؤلفون: Mahir Binici, Ayşegül Türkyılmaz, Gülbahar Güzel Erdal, Mahmut Balkan, Diclehan Oral, Selda Şimşek, Selahattin Tekes, İlyas Yücel, Zeynep Koca
المصدر: Volume: 5, Issue: 1 75-80
International Journal of Health Services Research and Policy
International Journal of Health Services Research and Policy, Vol 5, Iss 1, Pp 75-80 (2020)مصطلحات موضوعية: Gynecology, Infertility, Medicine (General), medicine.medical_specialty, 48/XXYY,infertility,klinefelter,azospermia, business.industry, General Medicine, klinefelter, medicine.disease, Tıp, azospermia, R5-920, Health Care Sciences and Services, 48/xxyy, Primary infertility, medicine, Medicine, Public aspects of medicine, RA1-1270, Sağlık Bilimleri ve Hizmetleri, infertility, business, Azospermia
وصف الملف: application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3877c437891c5897ecb337b6a35b249c
https://doi.org/10.33457/ijhsrp.681279 -
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المؤلفون: Tuğba Yüksel, Diclehan Oral, Esra Sizer
المصدر: Eastern Journal Of Medicine. 24:554-557
مصطلحات موضوعية: Genetics, business.industry, Ring chromosome, Medicine, Autism, General Medicine, business, medicine.disease
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المؤلفون: Uğur Keklikçi, Sedat Ava, Mine Karahan, Seyfettin Erdem, Diclehan Oral, Atılım Armağan Demirtaş
المساهمون: Dicle Üniversitesi, Tıp Fakültesi, Cerrahi Tıp Bilimleri Bölümü, Göz Hastalıkları Ana Bilim Dalı, Ava, Sedat, Karahan, Mine, Erdem, Seyfettin, Oral, Diclehan, Keklikçi, Uğur
مصطلحات موضوعية: Turkey, Sequence analysis, CYP1B1, DNA Mutational Analysis, Gene mutation, Genetic analysis, 03 medical and health sciences, Exon, 0302 clinical medicine, Optic Nerve Diseases, Medicine, Humans, Genetic Testing, PITX2, Gene, Myocilin, Genetics, business.industry, Glaucoma, eye diseases, Pedigree, body regions, Ophthalmology, Mutation (genetic algorithm), Mutation, 030221 ophthalmology & optometry, FOXC1, sense organs, business, Primary congenital glaucoma, 030217 neurology & neurosurgery, MYOC
وصف الملف: application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0978c156eb8aa8c5e21889cc8fff224c
https://hdl.handle.net/11468/10016 -
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المؤلفون: Selda Şimşek, Diclehan Oral, İlyas Yücel, Selahaddin Tekeş, Edip Unal
المصدر: Volume: 47, Issue: 2 482-491
Dicle Tıp Dergisi
Dicle Medical Journal, Vol 47, Iss 2, Pp 487-491 (2020)مصطلحات موضوعية: fish, Genetics, lcsh:R5-920, lcsh:R, Ring chromosome, lcsh:Medicine, Biology, karyotype, 13q deletion,Ring chromosome 13, Health Care Sciences and Services, Rare case, Sağlık Bilimleri ve Hizmetleri, lcsh:Medicine (General), 13q deletion, ring chromosome 13
وصف الملف: application/pdf
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المؤلفون: Hilmi Isi, Ayşegül Türkyılmaz, Selda Şimşek, Diclehan Oral, İlyas Yücel
المساهمون: MÜ, Sağlık Bilimleri Fakültesi, Beslenme Ve Diyetetik Bölümü, Türkyılmaz, Ayşegül, Dicle Üniversitesi, Tıp Fakültesi, Tıbbi Biyoloji ve Genetik AD, 0-Belirlenecek
المصدر: Dicle Medical Journal, Vol 45, Iss 2, Pp 219-222 (2018)
Volume: 45, Issue: 2 219-222
Dicle Tıp Dergisiمصطلحات موضوعية: lcsh:R5-920, General Mathematics, Klinefelter sendromu, kromozom anormalliği, hipergonadotropik hipogonadizm, lcsh:R, lcsh:Medicine, Hypergonadotrophic hypogonadism, Kromozom anormalliği, hipergonadotropikhipogonadizm, Health Care Sciences and Services, Hipergonadotropikhipogonadizm, Sağlık Bilimleri ve Hizmetleri, lcsh:Medicine (General), Klinefelter syndrome, Chromosomal abnormality, Genel ve Dahili Tıp
وصف الملف: application/pdf
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المؤلفون: Ayşegül Türkyılmaz, Selda Şimşek, Halit Akbas, Ahmet Yalinkaya, Turgay Budak, Diclehan Oral, Selahaddin Tekes
المصدر: Biotechnology & Biotechnological Equipment. 27:3829-3833
مصطلحات موضوعية: Pregnancy, Fetus, Pathology, medicine.medical_specialty, Amniotic fluid, business.industry, Obstetrics, Ultrasound, Chromosome, Prenatal diagnosis, Karyotype, medicine.disease, medicine, Trisomy, business, Biotechnology
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المؤلفون: M R Isik, B. Isık, Selda Şimşek, Diclehan Oral, Selahattin Tekes, Hasan Akkoc, Ayşegül Türkyılmaz
المصدر: Genetics and Molecular Research. 12:1392-1398
مصطلحات موضوعية: Male, Candidate gene, medicine.medical_specialty, Genotype, Peptidyl-Dipeptidase A, Gastroenterology, Pulmonary Disease, Chronic Obstructive, Gene Frequency, Internal medicine, Genetics, medicine, Humans, Allele, Molecular Biology, Gene, Allele frequency, Alleles, Aged, Sequence Deletion, COPD, Polymorphism, Genetic, business.industry, Smoking, Case-control study, Intron, General Medicine, Middle Aged, medicine.disease, Mutagenesis, Insertional, Case-Control Studies, Female, business
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b078d570def8c353b22539b168ecb2f3
https://doi.org/10.4238/2013.april.25.10
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