Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Turgay Budak"'
Autor:
Emin Kapi, Mehmet Fidanboy, Selcuk Otcu, Cihan Akgul Ozmen, Mahmut Balkan, Turgay Budak, M. Nuri Özbek
Publikováno v:
Journal of Pediatric Genetics. :205-208
Trisomy 8 is a relatively rare chromosomal abnormality. The majority of cases present with the mosaic form. Regular trisomy 8 is usually lethal and frequently results in miscarriage, while those with "trisomy 8 mosaicism" are more likely to survive.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1fe30d5bca256d2f0dbf774dc99fa32
https://doi.org/10.3233/pge-2012-032
https://doi.org/10.3233/pge-2012-032
Publikováno v:
Journal of Pediatric Genetics. :239-242
We report a case with different chromosome Y abnormalities. Case was an 11-year-old boy, who was diagnosed with short stature, referred to laboratory of human medical genetics laboratory for genetic evaluation. Chromosomal analysis of the case was ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a021f895d9e8573c0f2e78a681ae2151
https://doi.org/10.3233/pge-12038
https://doi.org/10.3233/pge-12038
Autor:
Turgay Budak, Mahmut Balkan, Hilmi Isi, M. Nail Alp, Mehmet Fidanboy, Sevgi Kalkanli, Halit Akbas
Publikováno v:
Journal of Pediatric Genetics. :243-246
We report a case of complete tetraploidy in amniotic fluid culture obtained at 17 wk of pregnancy. Amniocentesis was performed in this pregnancy because of a high-risk maternal serum screening result and abnormal ultrasound findings. Amniotic fluid w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52a8f8e20f0403934d8f21c565912876
https://doi.org/10.3233/pge-12039
https://doi.org/10.3233/pge-12039
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
Publikováno v:
Turkiye Klinikleri Journal of Medical Sciences. 32:1554-1559
Objective: We aimed to prospectively evaluate the effects of pegylated interferon alpha2a and alpha-2b therapy on chromosomal aberrations and mitotic index in patients with chronic hepatitis B. Material and Methods: Fifty patients with chronic hepati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e6390556bd9d8680e1b9bf7ba66b250
https://doi.org/10.5336/medsci.2011-26395
https://doi.org/10.5336/medsci.2011-26395
Publikováno v:
Turkish Journal of Obstetrics and Gynecology, Vol 7, Iss 2, Pp 145-148 (2010)
Balanced autosomal translocations are unusually observed in the patients with hypogonadotropic hypogonadism. The patient with hypogonadotropic hypogonadism had balanced reciprocal translocation involving chromosomes 8 and 9. The patient’s father, t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::3ee3b364160b358b87b787ae3e25f0ba
http://www.tjoddergisi.org/archives/archive-detail/article-preview/46-xx-del8q22-der9-t89q22p24-balanced-translocatio/9331
http://www.tjoddergisi.org/archives/archive-detail/article-preview/46-xx-del8q22-der9-t89q22p24-balanced-translocatio/9331
Publikováno v:
Journal of Genetic Counseling. 19:241-246
This study investigated parental decision-making to terminate or continue a pregnancy after prenatal diagnosis of a chromosomal abnormality among a sample of patients in Southeast Turkey. Between 2004 and 2007, 1068 amniocentesis tests were performed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::732a6319e5aa11f6f150123d3bd76278
https://doi.org/10.1007/s10897-009-9275-3
https://doi.org/10.1007/s10897-009-9275-3
Autor:
Mehmet Fidanboy, Turgay Budak, Abdullah Gedik, Ayşegül Türkyılmaz, Halit Akbas, Sevgi Kalkanli, Hilmi Isi, M N Alp, Selda Şimşek, Mahmut Balkan, Diclehan Oral
Publikováno v:
Genetics and Molecular Research. 9:1094-1103
We reviewed cytogenetic studies performed on 4216 patients who were referred to the Cytogenetics Unit at Dicle University Hospital, Diyarbair, Southeast Turkey, between 2000 and 2009. The cases were grouped according to the reason of referral for cyt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f9717d1c1ad46e337b56e47304efd6b0
https://doi.org/10.4238/vol9-2gmr827
https://doi.org/10.4238/vol9-2gmr827
Autor:
Hilmi Isi, S. Akdeniz, Selahattin Tekes, Mahmut Balkan, Tuba Gökdoğan Edgünlü, Mehmet Emin Erdal, Turgay Budak, Özlem İzci Ay, B. Sula, Diclehan Oral
Publikováno v:
Biotechnology & Biotechnological Equipment. 24:2014-2019
Behcet's disease (BD) is a chronic, multisystemic inflammatory disease. The specific etiology of BD remains elusive, but the interaction between infectious-agent exposure and genetic factors may have a role. In this report, we aim to investigate the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d6ff47209250b90775bdbf6705b89f4b
https://doi.org/10.2478/v10133-010-0055-x
https://doi.org/10.2478/v10133-010-0055-x
Publikováno v:
Dicle Medical Journal, Vol 35, Iss 1, Pp 65-68 (2008)
In this study, a case report is presented with Turner’s Syndrome with isochromosome carrier, Juvenile Osteoporosis and spontaneous fracture risk. As regards the case, who was referred to Genetic laboratory of Medical Biology Department, Medical Fac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::879589ae7359b11d608155b9cd5982b7
http://4181.indexcopernicus.com/fulltxt.php?ICID=887355
http://4181.indexcopernicus.com/fulltxt.php?ICID=887355