Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Diclehan ORAL"'
Autor:
Reyhan Gündüz, Rezan Buğday, Ahmet Yalinkaya, Diclehan Oral, Senem Yaman Tunç, Selahaddin Tekes
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://explore.openaire.eu/search/publication?articleId=doi_dedup___::261390d994e7d99c0c05e6f1c13d7ea2
https://doi.org/10.2399/prn.21.0291010
https://doi.org/10.2399/prn.21.0291010
Autor:
Mahir Binici, Ayşegül Türkyılmaz, Gülbahar Güzel Erdal, Mahmut Balkan, Diclehan Oral, Selda Şimşek, Selahattin Tekes, İlyas Yücel, Zeynep Koca
Publikováno v:
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)
International Journal of Health Services Research and Policy
International Journal of Health Services Research and Policy, Vol 5, Iss 1, Pp 75-80 (2020)
Klinefelter syndrome is a sex chromosomal aneuploidies with at least one extra X chromosome than normal male karyotype. The classic form of the 47 / XXY karyotype, the incidence of this syndrome is one in 500-1000 live male births. The incidence of 4
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3877c437891c5897ecb337b6a35b249c
https://doi.org/10.33457/ijhsrp.681279
https://doi.org/10.33457/ijhsrp.681279
The distribution of MEFV mutations in children FMF patients: Single center study in southeast Turkey
Publikováno v:
Volume: 49, Issue: 2 361-366
Dicle Tıp Dergisi
Dicle Tıp Dergisi
Amaç: Ailevi Akdeniz Ateşi (FMF), Akdeniz'de yaşayan etnik gruplarda (Türkler, Araplar, Yahudiler ve Ermeniler) görülen resesif geçişli otoinflamatuvar bir hastalıktır. Farklı coğrafi bölgelerde ve etnik gruplarda FMF’ deki MEFV mutasy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::69ea3111e758f28d690b85bb371ba718
https://hdl.handle.net/11468/9985
https://hdl.handle.net/11468/9985
Autor:
Diclehan Oral, Veysiye Hülya Üzel, Mehmet Akif Çürük, Selda Şimşek, Murat Söker, Selahaddin Tekes
Objectives 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 investi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9fdeb65ece4400a20264343b1d1b73b1
https://doi.org/10.1515/tjb-2020-0546
https://doi.org/10.1515/tjb-2020-0546
Publikováno v:
Eastern Journal Of Medicine. 24:554-557
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::114987a3786ef691d7b168ac2a0d20d9
https://doi.org/10.5505/ejm.2019.52714
https://doi.org/10.5505/ejm.2019.52714
Autor:
Uğur Keklikçi, Sedat Ava, Mine Karahan, Seyfettin Erdem, Diclehan Oral, Atılım Armağan Demirtaş
WOS:000630993900003 PMID: 33745036 Purpose To determine the common gene mutation in patients with primary congenital glaucoma (PCG) in the Southeast region of Turkey via genetic analysis and to evaluate whether there were other gene mutations in thes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0978c156eb8aa8c5e21889cc8fff224c
https://hdl.handle.net/11468/10016
https://hdl.handle.net/11468/10016
Publikováno v:
Volume: 47, Issue: 2 482-491
Dicle Tıp Dergisi
Dicle Medical Journal, Vol 47, Iss 2, Pp 487-491 (2020)
Dicle Tıp Dergisi
Dicle Medical Journal, Vol 47, Iss 2, Pp 487-491 (2020)
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 first case of ring c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c5851024539cbd91ab1c9ea818362cf
https://dergipark.org.tr/tr/pub/dicletip/issue/54760/755783
https://dergipark.org.tr/tr/pub/dicletip/issue/54760/755783
Publikováno v:
Dicle Medical Journal, Vol 45, Iss 2, Pp 219-222 (2018)
Volume: 45, Issue: 2 219-222
Dicle Tıp Dergisi
Volume: 45, Issue: 2 219-222
Dicle Tıp Dergisi
Klinefeltersendromu ilk tanımlanan kromozom bozukluğu olup temel olarak hipergonadotropikhipogonadizm ve önükoid vücut yapısı ile karakterizedir. Sıklığı 500-1000 canlı doğumda birdir. Klinefelter sendromunun genel özelliklerini uzun bo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4803b114fdb44590ccbee9c2dc80007a
https://hdl.handle.net/20.500.12809/8247
https://hdl.handle.net/20.500.12809/8247
Autor:
Ayşegül Türkyılmaz, Selda Şimşek, Halit Akbas, Ahmet Yalinkaya, Turgay Budak, Diclehan Oral, Selahaddin Tekes
Publikováno v:
Biotechnology & Biotechnological Equipment. 27:3829-3833
The aim of this study was to investigate the relationship between fetal abnormal karyotype and fetal abnormal ultrasound examination in pregnancy. A total of 191 women were analyzed for karyotyping after detection of a soft marker or of major malform
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b06d6a46955d2a6d2ef4c780c1ba15e9
https://doi.org/10.5504/bbeq.2013.0018
https://doi.org/10.5504/bbeq.2013.0018
Autor:
M R Isik, B. Isık, Selda Şimşek, Diclehan Oral, Selahattin Tekes, Hasan Akkoc, Ayşegül Türkyılmaz
Publikováno v:
Genetics and Molecular Research. 12:1392-1398
An insertion/deletion (I/D) polymorphism was identified in intron 16 of the gene encoding the human angiotensin I-converting enzyme (ACE), a candidate gene for chronic obstructive pulmonary disease (COPD). We investigated the relationship between thi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b078d570def8c353b22539b168ecb2f3
https://doi.org/10.4238/2013.april.25.10
https://doi.org/10.4238/2013.april.25.10