Medical Genetics

Prof. Dr. İlhan Sezgin

Doctor and researcher Medicana Bursa Bursa
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Which topics does this doctor work on?

From source

Medical areas of interest the doctor lists on their own profile on the institution’s website. Source: medicana.com.tr.

  • A1- Genetik Polimorfizim
  • A2- Mendelian Kalıtım
  • A3- Non-Mendelian Kalıtım
  • A4- Kalıtsal Metabolik Hastalıklar
  • A5- Prenatal Tanı ve Genetik Danışmanlık
  • A6- Popülâsyon Genetiği
  • A7-Konjenital Anomaliler
  • A8- Seksüel Gelişme Anomalileri
  • A9- Habitual Abortusların Genetik Nedenleri
  • A10-Muskuler Distrofiler
  • A11- Kondrodistrofiler
  • A12- Dismorfoloji
  • A13- Santral Sinir Sistemi Anomalileri
  • A14- Kalıtsal Metabolik Hastalıklar
  • A15- İnsan Davranış Genetiği
  • A16- Onkogenler
  • A17- Kalıtsal Kalp Hastalıkları
  • A18- X’e Bağlı Mental Retardasyon ve Frajil-X
  • A19- İmmünogenetik
  • B-Sitogenetik
  • A1- Lenfosit hücre kültürü ve kromozom analizi
  • A2- Kemikiliği stem hücre kültürü ve/veya direkt kromozom analizi
  • A3- Seks kromatin analizi
  • A4- Manuel ve otomatik karyotip, karyogram ve ideogram analizler
  • A5- G11, GT, GTG, C, Cd, BrdU, NOR, HRB ve T bantlama teknikleri
  • A6- Solid doku, CVS, Tahliye materyali, Amniyon hücre kültürleri
  • A7- Kordosentez hücre kültürü ve kromozom analizi
  • A8- Mikronukleus, SCE analizleri ve geno – sitotoksisite
  • A9- Karyometri, sitokaryometri
  • C- Moleküler Genetik
  • C1- Tıbbi Genetik Anabilim Dalında Moleküler Genetik ve Prenatal Tanı Laboratuarı kurmak ve yönetmek için bölümce gerekli hazırlıkları yapmayı yönetmek.

CV

Education and experience

From source

Experience

  • ExperienceYard. Doçent Dr. ; Cumhuriyet Üniversitesi Tıp Fakültesi, 1982 - SİVASmedicana.com.tr
  • ExperienceDoçent Dr. ; Cumhuriyet Üniversitesi Tıp Fakültesi, 1988 - SİVASmedicana.com.tr
  • ExperienceProf Dr. ; Cumhuriyet Üniversitesi Tıp Fakültesi, 1993 - SİVASmedicana.com.tr

Education

  • 1976Ege Üniversitesi Tıp Fakültesimedicana.com.tr
  • 1980Ege Üniversitesi Tıp Fakültesi, Pediatri/Tıbbi Genetikmedicana.com.tr

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  • SpecialtyMedical Geneticsmedicana.com.trFrom source
  • InstitutionMedicana Bursamedicana.com.trFrom source
  • Publications15 publicationsmedicana.com.tr profile pageFrom source
  • Last synchronised7 November 2026 03:18https://www.medicana.com.tr/hekim-detay/12315/ilhan-sezginmedicana.com.tr

Scientific work

Publications

15 publications

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

    Source: medicana.com.tr profile page

  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)

    Source: medicana.com.tr profile page

  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)

    Source: medicana.com.tr profile page

  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)

    Source: medicana.com.tr profile page

  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)

    Source: medicana.com.tr profile page

  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)

    Source: medicana.com.tr profile page

  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)

    Source: medicana.com.tr profile page

  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)

    Source: medicana.com.tr profile page

  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)

    Source: medicana.com.tr profile page

  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).

    Source: medicana.com.tr profile page

View all 15 publications