Bilimsel çalışmalar

Prof. Dr. İlhan Sezgin

15 yayın. Her yayının yanında bilginin kaynağı yazar.

Profile dön

  1. 867,51.SEZGIN I and ATALAY A : The Effect of Nitrosopyrolidine On Human Lymphocyte Chromosomes. J. Health Sci., 7: 29-35, 1995. (100)

    Kaynak: medicana.com.tr profil sayfası

  2. 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)

    Kaynak: medicana.com.tr profil sayfası

  3. 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)

    Kaynak: medicana.com.tr profil sayfası

  4. 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)

    Kaynak: medicana.com.tr profil sayfası

  5. 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)

    Kaynak: medicana.com.tr profil sayfası

  6. 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)

    Kaynak: medicana.com.tr profil sayfası

  7. 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)

    Kaynak: medicana.com.tr profil sayfası

  8. 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)

    Kaynak: medicana.com.tr profil sayfası

  9. 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)

    Kaynak: medicana.com.tr profil sayfası

  10. 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).

    Kaynak: medicana.com.tr profil sayfası

  11. 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)

    Kaynak: medicana.com.tr profil sayfası

  12. 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)

    Kaynak: medicana.com.tr profil sayfası

  13. 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)

    Kaynak: medicana.com.tr profil sayfası

  14. 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)

    Kaynak: medicana.com.tr profil sayfası

  15. 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

    Kaynak: medicana.com.tr profil sayfası