Browsing by Author "Sezgin I."
Now showing items 1-10 of 10
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Analysis of HumFABP2 as a polymorphic human genetic marker in the Turkish population
Beyaztas F.Y.; Sezgin I.; Gul E.; Erkol Z. (2007)Objectives: To examine the allele frequencies of HumFABP2 locus in 155 individuals from different regions of Turkey. Methods: The study was carried out in Cumhuriyet University Hospital, Sivas, Turkey, between March and ... -
C, G and Restriction Endonuclease (Alu I, Nhe I, Hae III, Mbo I, Hinf I) Banding of the Chromosomes in Chalcalburnus tarichi (PALLAS 1811) Endemic to Lake Van [Van Gölüne Endemik Olan İnci Kefali (Chalcalburnus tarichi PALLAS 1811) Kromozomlarinin C, G ve Restriksiyon Endonükleazlar (Alu I, Nhe I Hae III, Mbo I Hinf I) ile Bantlanmasi]
Gül S.; Çolak A.; Sezgin I.; Kalo?lu B. (2003)Karyotype analysis was performed in Chalcalburnus tarichi specimens by investigating the number and structures of their chromosomes. The fish used in this study were caught with fishing nets from Lake Van and taken to the ... -
A Case of bisatellited-isodicentric supernumerary chromosome 15
Süngü S.; Karaman B.; Ferda Perçin E.; Balci S.; Sezgin I. (2001)[No abstract available] -
A case with popliteal pterygium syndrome and its surgical treatment
Barutçu A.; Midoğlu H.; Köstem L.; Sezgin I. (Springer-Verlag, 1990)Popliteal pterygium syndrome is a rare congenital anomaly. The literature contains only a few reports about treatment of this malformation. This paper outlines our approach in one case and compares our surgical technique ... -
Complete androgen insensitivity syndrome with 45,XY,t(13q;14q) translocation (two cases)
Özdemir Ö.; Süngü S.; Perçin E.F.; Sezgin I. (2002)We report 2 cases of complete androgen insensitivity syndrome from 1 family with 45,XY,t(13q;14q) karyotype including complete testicular feminisation (TF) clinical features. The chromosomal translocation is not generally ... -
The fetal hydantoin syndrome.
Oguz A.; Sezgin I.; Gökalp A.; Gültekin A. (1991)[No abstract available] -
MCP-1-2518 AZ>G and CCR2 V64I polymorphisms in Turkish patients with lung cancer
Bagci B.; Arslan S.; Kurtulgan H.K.; Sezgin I.; Yildirim M.E.; Bagci G. (2016)In the current study, we aimed to investigate the possible role of MCP-1-2518 A>G and CC chemokine receptor 2 (CCR2) V64I polymorphisms in patients with lung cancer. Sixty-five patients with lung cancer (57 with NSCLC and ... -
A new syndrome with cardiac malformation, cleft lip?palate, microcephaly and digital anomalies?
Perçin E.F.; Düzcan F.; Kafali G.; Sezgin I. (1995)A family with cardiac malformation, cleft lip?palate, short stature, microcephaly, distally placed thumbs, short 2nd and 5th fingers, long and broad 1st toes, broad distance between 1st and 2nd toes and mediodorsal curvature ... -
Noonan's syndrome with simple partial syndactyly of the fingers and bilateral cubital webs.
Undar L.; Gultekin A.; Yilmaz M.B.; Sezgin I. (1990)[No abstract available] -
Underorganisation of chromatin structure in human metaphase chromosomes by induction of 5-aza-2'-deoxycytidine (Decitabine) [Baz analogu 5-aza-2'-deoksisitidin (Desitabin) in insan kromozomlarinda neden oldugu kromatin organizasyon bozukluklari]
Ozdemir O.; Sezgin I.; Colak A. (Gulhane Askeri Tip Akademisi, 1998)Human metaphase chromosomes were exposed to different concentrations (10-8-10-2 M) of 5-aza-2'-deoxycytidine, a DNA methyl inhibitor, in order to determine the in vivo effect of the agent on chromosome packaging. It has ...