Zobrazeno 1 - 10
of 57
pro vyhledávání: '"ORAL, Diclehan"'
Autor:
Gündüz, Reyhan, Yaman Tunc, Senem, Buğday, Rezan, Oral, Diclehan, Tekeş, Selahaddin, Yalınkaya, Ahmet
Publikováno v:
Perinatal Journal, Vol 29, Iss 1, Pp 63-70 (2021)
Objective The aim is to contribute to the literature by carrying out retrospective analysis of the cases who underwent amniocentesis in our clinic and sharing our relevant experience. Methods A total of 632 cases who underwent amniocentesis in the se
Externí odkaz:
https://doaj.org/article/04011044d03a4a08a689c2377c1603b4
Autor:
Tekeş Selahaddin, Oral Diclehan, Söker Murat, Şimşek Selda, Uzel Veysiye Hülya, Çürük Mehmet Akif
Publikováno v:
Türk Biyokimya Dergisi, Vol 47, Iss 1, Pp 113-118 (2021)
Hemoglobin disorders are quite heterogeneous in the Turkish population. Up to now, more than forty different beta thalassemia mutations and 60 hemoglobin variants have been characterized in the country. The aim of this study was to investigate geneti
Externí odkaz:
https://doaj.org/article/92208815437d47b5a55e564480910532
Autor:
ÇALIŞKAN, Lütfiye Gül, BALKAN, Mahmut, TEKEŞ, Selahattin, ORAL, Diclehan, BİNİCİ, Mahir, YÜCEL, İlyas
Publikováno v:
Volume: 5, Issue: 2 44-50
Ege Tıp Bilimleri Dergisi
Aegean Journal of Medical Sciences
Ege Tıp Bilimleri Dergisi
Aegean Journal of Medical Sciences
Objective: Hematological cancers are a group of neoplasms that affect the bone marrow, blood and lymph nodes, usually associated with structural and numerical chromosomal abnormalities. Bone marrow examination in hematological cancers has an illumina
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=tubitakulakb::fca35960bb5a17e6c81b0808f5845fb7
https://dergipark.org.tr/tr/pub/egetbd/issue/72431/1118486
https://dergipark.org.tr/tr/pub/egetbd/issue/72431/1118486
Autor:
Gündüz, Reyhan, Tunç, Senem Yaman, Buğday, Rezan, Oral, Diclehan, Tekeş, Selahaddin, Yalınkaya, Ahmet
Amaç: Kliniğimizdeki amniyosentez uygulanan olguların retrospektif analizini yapmak ve bu konudaki deneyimimizi paylaşarak literatüre katkı sunmaktır.Yöntem: Çalışmamıza ikinci trimesterde amniyosentez uygulanan 632 olgu dahil edildi. Olg
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3346::3c7aab5089622efb2d3b4f8c58c83385
https://hdl.handle.net/11468/10025
https://hdl.handle.net/11468/10025
Autor:
Oral, Diclehan1 diclehan.oral@dicle.edu.tr, Şimşek, Selda1, Türkyılmaz, Ayşegül2, Yücel, İlyas1, İsi, Hilmi1
Publikováno v:
Dicle Medical Journal / Dicle Tip Dergisi. Jun2018, Vol. 45 Issue 2, p219-222. 4p.
Autor:
ORAL, Diclehan, BALKAN, Mahmut, TEKEŞ, Selahattin, YÜCEL, İlyas, GÜZEL ERDAL, Gülbahar, BİNİCİ, Mahir, KAVAK, Fikriye Fulya
Publikováno v:
Volume: 13, Issue: 1 42-46
International Archives of Medical Research
International Archives of Medical Research
Objective: Structural chromosomal abnormalities such as translocation in males and y deletions in the molecular missile cause infertility and related azoospermia. The aim of this study was to perform the karyotype analysis of a 51-year-old male patie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=tubitakulakb::7099613b2d4a7f6055255696665f5ae8
https://dergipark.org.tr/tr/pub/iamr/issue/62986/893696
https://dergipark.org.tr/tr/pub/iamr/issue/62986/893696
Autor:
YÜCEL, İlyas, BİNİCİ, Mahir, KAVAK, Fikriye Fulya, ORAL, Diclehan, TEKEŞ, Selahattin, BALKAN, Mahmut
Publikováno v:
Volume: 12, Issue: 2 7-15
International Archives of Medical Research
International Archives of Medical Research
Objective: The main aim of this study was to examine the effects of dimethyl sulfoxide (DMSO) on chromosomal abnormalities in human peripheral blood lymphocytes.Methods: Peripheral blood samples were collected from two healthy men and two healthy wom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=tubitakulakb::5b106c9baf371afe10584c4a9eed0865
https://dergipark.org.tr/tr/pub/iamr/issue/58526/808257
https://dergipark.org.tr/tr/pub/iamr/issue/58526/808257
This case report describes the cytogenetic and molecular characterization of a child with de-novo ring chromosome 13[r(13)]. The child presented with short stature, growth retardation and a Turner syndrome diagnosis. She was the firstcase of ring chr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3566::260379951357beedd45225ba8537542b
Akademický článek
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Autor:
Tekeş, Selahaddin, Oral, Diclehan, Söker, Murat, Şimşek, Selda, Uzel, Veysiye Hülya, Çürük, Mehmet Akif
Publikováno v:
Turkish Journal of Biochemistry / Turk Biyokimya Dergisi; Feb2022, Vol. 47 Issue 1, p113-118, 6p