Prof. Dr. İlhan Sezgin

867,51.SEZGIN I and ATALAY A : The Effect of Nitrosopyrolidine On Human Lymphocyte Chromosomes. J. Health Sci., 7: 29-35, 1995. (100)

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2.SEZGIN I and OZDEMIR O: A New Methodic Approach in the Analysis of the Centromer Heterochromatin Index of Human Chromozome No 1 in the Population using the C-Band Technique. J Health Sci., 7: 36-41, 1995. (100)

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3.PERÇİN EF, DÜZCAN F, KAFALI G, SEZGİN İ : A New Syndrome with Cardiac Malformation, Cleft Lip-Palate, Microcephaly and Digital Anomalies. Clinical Genetics, 48: 264-267, 1995. (97,5)

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4.PERÇİN EF, PERÇİN S, EGİLMEZ H, SEZGİN İ, ÖZBAŞ F, AKARSU NA : Mesoaxial Complete Syndactyly and Synostosis with Hypoplastic Thumbs: an Unusual Combination or Homozygous Expression of Syndactyly Type I?. Journal of Medical Genetics, 34: 868-874, 1998. (67,5)

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5.SEZGIN I, SUNGU S, BEKAR E, CETIN M, CERAN H : Cyclopia-astomia-agnathia-holoprosencehaly assosication: a case report, Clinical Dysmorphology, 11:225-226, 2002. (120)

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6.ERGUR AT, TAS F, YILDIZ E, KILIC F, SEZGIN I: Meckel-Gruber syndrome associated with gastrointestinal tractus anomaly. Turk J. Pediatr. 2004 Oct-Dec; 46(4):388-92. PMID: 15641280. (A1) (90)

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7.GUL S, COLAK A, SEZGIN I, KALOGLU B : “Karyotype Analysis in Alburnus heckeli (BATTALGIL,1943) From the Lake Hazer”, Turk J Vet Anim Sci, 28,309-314, 2004. (97,5)

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8.ÖZDEMİR Ö, GÜL E, KILIÇARSLAN H, GÖKÇE G, BEYASTAŞ FY, AYAN S, SEZGİN İ : SRY and AZF gene variation in male infertility: A cytogenetic and molecular approach. International Urol and Nephrol.39:1183-1189,2007.(82,5)

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9.BEYAZTAŞ FY, SEZGİN İ, GÜL E, ERKOL Z : Analysis of HumFABP2 as Polymorphic Human Genetic Marker in Turkish Population, Saudi Medical Journal,28(10),1493-1495, 2007.(112,5)

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10.BEREKET A, TURAN S, ELCIOGLU N, HACIHANEFIOGLU S, MEMIOGLU N, BAS F, BUNDAK R, DARENDELILER F, GUNOZ H, SAKA N, ERCAN O, ARSLANOGLU I, ISGUVEN P, YILDIZ M, CAN S, OZERKAN E, COKER M, DARCAN S, OZKAN B, ORBAK Z, OZTAS S, ALANDUZ S, SEZGIN I, ATABEK E, ERKUL I, AKYUREK C, ERDOGAN G Adult height in Turkish patients with Turner syndrome without growth hormone treatment,The Turkish Jurnal Pediatrics, 50:415-417,2008(60P).

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Katrancioglu N, Manduz S, Karahan O, Yilmaz MB, Sezgin I, Bagci G, Berkan O The role of the CCR2 gene polymorphism in abdominal aortic aneurysms. Angiology. 2011;62(2):140-3.(60p)

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Ozdemir O, Sezgin I, Kurtulgan HK, Candan F, Koksal B, Sumer H, Icagasioglu D, Uslu A, Yildiz F, Arslan S, Cetinkaya S, Citli S, Oztemur Z, Kayatas M. Prevalence of known mutations in the MEFV gene in a population screening with high rate of carriers.Mol Biol Rep. 2010 Feb 18.(112.50p)

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Toker AS, Ay S, Yeler H, Sezgin I.Dental findings in Cornelia de Lange syndrome. Yonsei Med J. 2009 Apr 30;50(2):289-92.(82.5p)

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SEZGIN I, KOKSAL B, BAGCI G, KURTULGAN HK, OZDEMIR O. CCR2 polymorphism in chronic renal failure patients that requiring long-term haemodialysis. Intern. Med. 2011.(120p)

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Bagci B, Bagci G, Candan F, Ozdemir O, SEZGIN I. The protective effect of MCP-1-2518 A> G promoter polymorphism in Turkish chronic renal failure patients requiring long-term hemodialysis. International Urology and Nephrology 47(3), 551-556, 2015

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