Kurslar, Kongresslar, Konferensiyalar va Ta’limlar
Intergen o‘zi tashkil etayotgan kurslar, kongresslar, konferensiyalar va ta’lim dasturlari orqali ilmiy faoliyatni keng ommalashtirish yo‘lidagi faoliyatini davom ettirmoqda.
1- Behchet kasalligi bo‘lgan, ko‘z zararlanishi mavjud va mavjud bo‘lmagan bemorlarda O‘rta yer dengizi isitmasi (MEFV) geni mutatsiyalari.
Nilüfer Yalçındağ, Yeşim Gedik-Oğuz, Serdar Ceylaner 12-Xalqaro Ko‘z Yallig‘lanishlari Jamiyati Kongressi, 2-Xalqaro Ko‘z Yallig‘lanishlari Jamiyatlari Assambleyasi, 27-Ispan Uveit Tadqiqot Guruhi Yig‘ilishi, 27–28-fevral va 1-mart.
2- O‘ziga shikast yetkazish va buyrak toshlari: qisman va to‘liq Lesch-Nyhan sindromiga ega ikki bemor haqida klinik holat.
Neslihan Önenli Mungan, Deniz Kör, Aysun Karabay Beyazıt, Serdar Ceylaner, Sevcan Erdem, Faruk İncecik, Ali Anarat Türk Ped Arş 2013 Maxsus soni; 16-172
3- Erta davrda dismorfik belgilar asosida tashxis qo‘yilgan Smith-Lemli-Opitz sindromi holati.
İlyas Okur, Mehmet Gündüz, Fatma Güzel, Nevra Koç, Fevziye Başkan Vuralkan, Serdar Ceylaner Türk Ped Arş 2013 Maxsus soni; 16-172
4- TAR sindromi tashxisi aCGH tahlili bilan tasdiqlandi.
S. Ceylaner, Y. K. Terzi, S. Kalyoncu, F. I. Sahin. ASHG Yillik Yig‘ilishi, San-Fransisko, Kaliforniya, 2012-yil 6–10-noyabr.
5- Endotelial azot oksidi sintazasi geni 894 G>T va 786 T>C polimorfizmlari endometrioz uchun xavf omilimi?
Ayranci, H.; Dogan, H.; Ceylaner, S. XX FIGO Ginekologiya va Akusherlik Jahon Kongressi, International Journal of Gynecology and Obstetrics, 2012-yil oktyabr, 119-qo‘shimcha 3:S327-S328
6- “Journal of Clinical Research in Pediatric Endocrinology” 2011-yilning eng yaxshi klinik holat mukofoti – Tireotropin retseptori genidagi A623V germinal mutatsiyasi tufayli kuzatilgan sporadik autoimmun bo‘lmagan neonatal gipertireoz.
Aycan Z, Ceylaner S, Yılmaz Ağdıoğlu S, Çetinkaya S, Başkan VN, Peltek Kendirci HN
7- 9p delesiya sindromiga ega bemorda tanglay yorig‘i,
Far, Asli Subasioglu; Ceylaner, Serdar; Erdogan, Murat; Karabulut, Yesim; Balta, Burhan; Bahadir, Oguzhan; Kurt, Fatima; Dogan, Muhammed; Dundar, Munis. European Biotechnology Congress 2011, Current Opinion in Biotechnology 2011 22 Supplement 1:S106
8- Homilada teri osti shishiga sabab bo‘luvchi ensa shishi, kistoz gigroma va immun bo‘lmagan gidropsning xromosoma anomaliyalari bilan bog‘liqligi.
D.C. Arıkan, A. Coskun, G. Kıran, H. Kıran, M.A. Güven, S. Turk Onalik, Homila Tibbiyoti va Perinatologiya Jamiyatining 7-Milliy Kongressi, Istanbul, Turkiya, 2010-yil sentyabr.
9- Terminal ko‘ndalang qo‘l-oyoq nuqsonlari va ular bilan bog‘liq sindromlarning asosiy sababi trombofiliyadir. Prospektiv tadqiqot natijalari.
S. Ceylaner, G. Ceylaner, Acar K., Gul D., Zencirlioğlu A., Okumuş N. Turk Tibbiy Genetika Jamiyatining xalqaro ishtirokdagi 9-Milliy Tibbiy Genetika Kongressi. Istanbul, 2010-yil 1–5-dekabr. Clinical Genetics 2010 78 (1)
10- Qo‘shni gen buzilishlari har doim ham “qo‘shni genlar sindromi” emas: uch xil genetik kasallikka ega bir holatdan olingan saboqlar.
Aslan D., G. Ceylaner., S. Ceylaner. Turk Tibbiy Genetika Jamiyatining xalqaro ishtirokdagi 9-Milliy Tibbiy Genetika Kongressi. Istanbul, 2010-yil 1–5-dekabr. Clinical Genetics 2010 78 (1)
11- Amniotik suyuqlik hujayralari kulturasi va shprits toksikligi.
G. Ceylaner., M.A. Güven, S. Ceylaner., Ekerbiçer H. Turk Tibbiy Genetika Jamiyatining xalqaro ishtirokdagi 9-Milliy Tibbiy Genetika Kongressi. Istanbul, 2010-yil 1–5-dekabr. Clinical Genetics 2010 78 (1)
12- Osteogenesis imperfecta 2-tipi: prenatal 2B, 3B ultratovush va postnatal 3B KT topilmalari.
Güzelmansur İ., Şahin E., Ceylan N., G. Ceylaner. 30-Milliy Radiologiya Kongressi, Antaliya, 2009-yil 4–9-noyabr.
13- Radial ray malformatsiyasi. Prenatal 2B, 3B ultratovush va postnatal 3D KT topilmalari.
Güzelmansur İ., Şahin E., Ceylan N., G. Ceylaner. 30-Milliy Radiologiya Kongressi, Antaliya, 2009-yil 4–9-noyabr.
14- Prenatal tashxisda QF-PCR yoki FISH usuli yetarlimi? Amniotik suyuqlikda xromosoma anomaliyasi aniqlangan 417 holat tahlili.
Gül D., S. Ceylaner., G. Ceylaner. 12-Milliy Perinatologiya Kongressi, Antaliya, 2009-yil 23–26-aprel.
15- Xromosoma anomaliyasi aniqlangan homiladorlikni yakunlash materiallarining 163 ta holati tahlili.
Gül D., S. Ceylaner., G. Ceylaner. 12-Milliy Perinatologiya Kongressi, Antaliya, 2009-yil 23–26-aprel.
16- Trisomiya 3 ning prenatal tashxisi: klinik holat.
Arıkan D.C., Coşkun A., Kıran G., G. Ceylaner. 12-Milliy Perinatologiya Kongressi, Antaliya, 2009-yil 23–26-aprel.
17- Terminal ko‘ndalang qo‘l-oyoq nuqsonlarining eng ko‘p uchraydigan sababi trombofiliyadir. Prospektiv tadqiqot natijalari.
G. Ceylaner., S. Ceylaner., Acar K., Gül D., Zencirlioğlu A., Okumuş N. 7-Milliy Pediatrik Gematologiya Kongressi, Anqara, 2009-yil 24–27-may.
18- Pediatrik gematologik saratonlarda genetik yondashuv va yangi usullarning hissasi.
S. Ceylaner., G. Ceylaner., Gül D. 7-Milliy Pediatrik Gematologiya Kongressi, Anqara, 2009-yil 24–27-may.
19- Osteogenesis imperfecta 2-tipi: prenatal 2B, 3B ultratovush va postnatal 3B KT topilmalari.
Güzelmansur İ., Şahin E., Ceylan N., G. Ceylaner. 30-Milliy Radiologiya Kongressi, Antaliya, 2009-yil 4–9-noyabr.
20- Radial ray malformatsiyasi. Prenatal 2B, 3B ultratovush va postnatal 3D KT topilmalari.
Güzelmansur İ., Şahin E., Ceylan N., G. Ceylaner. 30-Milliy Radiologiya Kongressi, Antaliya, 2009-yil 4–9-noyabr.
21- Trombofiliya terminal ko‘ndalang qo‘l-oyoq nuqsonlarining eng ko‘p uchraydigan sababidir: prospektiv tadqiqot natijalari.
Gülay Ceylaner, Serdar Ceylaner, Kadir Acar, Davut Gül, Ayşegül Zencirlioğlu, Nurullah Okumuş. 7-Milliy Pediatrik Gematologiya Kongressi, 2009-yil 24–27-may, Anqara.
22- Pediatrik gematologik saratonlarda umumiy genetik yondashuv va yangi usullarning hissasi.
Serdar Ceylaner, Gülay Ceylaner, Davut Gül. 7-Milliy Pediatrik Gematologiya Kongressi, 2009-yil 24–27-may, Anqara.
23- Neu-Laxova sindromi: klinik holat.
Mutlu B, Narlı N, Özcan K, Ceylaner S, Yıldıztaş H, Satar M. 17-Milliy Neonatologiya Kongressi, 2009-yil 27–30-aprel, Cheshme, Izmir, 224-bet.
24- Amniotsentez holatlarining retrospektiv baholanishi.
Coskun, D. C. Arıkan, G. Kıran, M. A. Güven, B. Köstü, S. Ceylaner. 12-Milliy Perinatologiya Kongressi, Antaliya, Turkiya, 2009-yil aprel.
25- Takrorlanuvchi homiladorlik yo‘qotilishlarida Factor V (G1691A), Protrombin (G20210A) va Metilentetrahidrofolat reduktaza (C677T) geni polimorfizmlarini o‘rganish.
European Human Genetics Conference, 2008-yil 31-may–3-iyun (Samli H., Imirzalioglu N., Koken G., Ceylaner G., Ceylaner S. bilan).
26- Mitral qopqoq prolapsi bilan bog‘liq piknodizostoz: ikki aka-uka (opa-singil) haqida klinik holat.
Esma Altınel, Aysel Yöney, Saliha Şenel, Nilgün Erkek, Candemir Karacan, Utku Arman Örün, Serdar Ceylaner. 4-Uludağ Pediatrik Qish Kongressi, 2008-yil 18–19-mart.
27- Güven E.S.G, Ceylaner S, Çınar Ö, Dilbaz S, Aydın S, Gürsoy S, Haberal A. Oligoasteno-teratozoospermiya bilan kechgan erkakda 46, XY, i(9)(P10), i(9)(Q10) kariotip anomaliyasi va davolashdan keyingi qaytuvchanlik. Reproduktiv Endokrinologiya va Bepushtlik bo‘yicha 3-Milliy Kongress, Antaliya, 2008-yil 16–19-oktabr.
28- Rubinstein-Taybi sindromiga ega klinik holat.
Kuraş Can Y, Erdoğan F., Ceylaner S., Çelik A., Özdemir O., Yılmaz G. 51-Milliy Pediatriya Kongressi, 2007.
29- I-tip thanatoforik displaziyaning prenatal tashxisi: ultratovush va biokimyoviy topilmalar.
Erdemoğlu, E., T. Mungan, S. Ceylaner va M. Tezimer. Akusherlik va ginekologiyada ultratovush bo‘yicha 31-Ilg‘or kurs, 2006-yil 19–20-may, Antaliya. Ultrasonography in Obstetrics and Gynecology 6(1-2), S56.
30- Chuqur vena trombozida irsiy trombofilik omillarning roli.
Bardakcı, H., G. Ceylaner, S. Ceylaner, Kervan Ü., Tuncel Ç., Birincioğlu L. 13-Milliy Qon Tomir Jarrohligi Kongressi, 2007-yil 22–26-may.
31- Homiladorlikning 12+3 haftasida NT oshishi bilan namoyon bo‘lgan va DORV hamda VSD tashxisi bilan birga kechgan Trisomiya 18 holati.
Güven M.A., G.S. Ceylaner, A. Coşkun. Akusherlik va Ginekologiya Ultratovushi bo‘yicha 5-Kongress, Antaliya, 2006.
32- Prenatal tashxis qo‘yilgan Cantrell pentalogiyasi holati.
Güven M.A., G.S. Ceylaner, A. Coşkun. Akusherlik va Ginekologiya Ultratovushi bo‘yicha 5-Kongress, Antaliya, 2006.
33- Prenatal tashxis qo‘yilgan Kampomelik displaziya holati.
Güven M.A., G.S. Ceylaner, A. Coşkun. Akusherlik va Ginekologiya Ultratovushi bo‘yicha 5-Kongress, Antaliya, 2006.
34- Tik turgan ektrodaktiliya bilan kechgan letal ko‘p pterigium sindromi.
G. Ceylaner, M.A. Güven, S. Ceylaner, A. Coşkun. Akusherlik va Ginekologiya Ultratovushi bo‘yicha 5-Kongress, Antaliya, 2006.
35- Yuqori qo‘l pterigiyalari bilan namoyon bo‘lgan va prenatal tashxis qo‘yilgan Bartsocas-Papas sindromi.
G. Ceylaner, M.A. Güven, S. Ceylaner, A. Coşkun. Akusherlik va Ginekologiya Ultratovushi bo‘yicha 5-Kongress, Antaliya, 2006.
36- Prenatal tashxis va o‘limdan keyingi baholash natijalari.
S. Ceylaner, Eserdağ S., G. Ceylaner, Danışman N. Prenatal Tashxis va Tibbiy Genetika bo‘yicha VII Milliy Kongress. Kayseri, 2006-yil 17–20-may.
37- Gipogonadizm belgilari kuzatilgan bir tuxumli egizaklar.
G. Ceylaner, Aktürk M., Şahin İ., S. Ceylaner, Mollamahmutoğlu L. Prenatal Tashxis va Tibbiy Genetika bo‘yicha VII Milliy Kongress. Kayseri, 2006-yil 17–20-may.
38- Autosomal retsessiv imperforatsiyalangan qizlik pardasi.
G. Ceylaner, S. Ceylaner, Akın Su F., Mollamahmutoğlu L. Prenatal Tashxis va Tibbiy Genetika bo‘yicha VII Milliy Kongress. Kayseri, 2006-yil 17–20-may.
39- EMANUEL sindromi (qo‘shimcha der(22) sindromi) holatining prenatal tashxisi.
M.A. Güven, G. Ceylaner, S. Ceylaner, A. Coşkun. Akusherlik va Ginekologiyada Ultratovush bo‘yicha 16-Jahon Kongressi, London, Buyuk Britaniya, 2006-yil 3–7-sentyabr.
40- Mohr sindromining prenatal tashxisi.
M.A. Güven, G. Ceylaner, S. Ceylaner, M. Uzel, A. Coşkun. Akusherlik va Ginekologiyada Ultratovush bo‘yicha 16-Jahon Kongressi, London, Buyuk Britaniya, 2006-yil 3–7-sentyabr.
41- Prenatal tashxis qo‘yilgan va tug‘ilgandan keyin tasdiqlangan Saldino-Noonan sindromi holati.
M.A. Güven, S. Ceylaner, M. Uzel, A. Coşkun, G. Ceylaner. XX Yevropa Perinatal va Neonatal Tibbiyot Kongressi, Praga, 2006-yil 24–27-may.
42- Trisomy 4 p syndrome: clinical similarities with De Lange syndrome
G. Ceylaner, S. Ceylaner, N. Consultant, L. Mollamahmutoğlu. European Human Genetics Conference 2005, Prague, Czech Republic, 7-10 May 2005
43- A case of fetal anticonvulsant syndrome with a severe bilateral upper limb defect
M.A. Guven, C. Batukan, S. Ceylaner, G. Ceylaner, M. Uzel. International forum on birth, P 20, 8-11 June, Rome, 2005.
44- Prenatal diagnosis of Meckel Gruber Syndrome presenting with renal agenesis: report of a case.
M.A. Guven, S. Ceylaner, G. Ceylaner, I.E. Ertas, VI. International Congress of the Turkish-German Gynecology Association, Arch Gynecol Obstet (suppl 1), 271, 2005, MFM&P-047, 19-22 May, Antalya, 2005.
45- Prenatal diagnosis of 14q duplication caused by crossing over in paternal pericentric inversion.
Bagci G, Ozcan Caliskan M, Keser I, Ozturk S, Mendilcioglu I, Ceylaner S, Zergeroglu S, Luleci G. Fetal Medicine; Prenatal Diagnosis 2005, 30 April- 02 May 2005, Antalya, Proceedings Book: P16, p:76, 2005.
46- Short rib polydactyly syndrome type II (Majewski syndrome): A case report
Kelekçi, S., Yılmaz, B., Kaya, E., Ceylaner, S., Consultant, N., Mollamahmutoğlu, L. Perinatal Medicine Congress- 2005, 1-5 October Kuşadası, Turkey, 2005
47- Prenatal diagnosis with amniocentesis and cordocentesis: Evaluation of 181 cases.
Güven, M. A., Ceylaner, S. 10. National Perinatology Congress & International workshop on multiple pregnancies, P-90, 10-13 April, Istanbul, 2005.
48- Lower mesodermal defect sequence: a case report
Tos, T., İkbal, M. , Aktaş, S. , Avcı, M. , Ceylaner, S VI. National Congress of Prenatal Diagnosis and Medical Genetics. Belek, Antalya, 21-24 April 2004
49- Relationship between recurrent miscarriages and x-inactivation
Başğışlar, G. S. , Söylemez, F. , Cengiz, B. , Üstüner, I. , Ceylaner, S. , Ceylaner, G. , Özçelik, T. , Acar, AI. National Congress of Prenatal Diagnosis and Medical Genetics. Belek, Antalya, 21-24 April 2004
50- The diagnosis of hypoplastic left heart syndrome by using four heart chamber view at 17 weeks of gestation.
Güven, M. A., Ceylaner, S., Çıragil, G. 4th National Gynecology & Obstetrics Congress, P-17, 20-25 April, Antalya, 2004 (Oral presentation).
51- A case with dextrocardia and multiple cardiac anomalies; Prenatal diagnosis and postnatal evaluation.
Ceylaner, S., M. A. Güven, G. Çıragil, S. Zengeroğlu 4th National Congress of Gynecology & Obstetrics, P-18, 20-25 April, Antalya, 2004 (Oral presentation).
52- Prenatal diagnosis of thoraco-omphalophagus conjoined twins at 13 weeks of pregnancy: a case report.
Kıran, G., Kiran, H., Güven, A. M., Ceylaner, S., Karakuş, S. 4th Obstetric, and Gynecological Ultrasonography Congress, Harbiye Military Museum, Istanbul, 6-9 October 2004
53- A case of enteric duplication cyst located in the posterior mediastinum, diagnosed prenatally.
Güven, M. A. , Gülgösteren, M. , Ekiz, S., Ceylaner, S. , Çıragil, G4. Obstetric and Gynecological Ultrasonography Congress, Harbiye Military Museum, Istanbul, 6-9 October 2004
54- Evaluation of two cases with Dandy-Walker malformation and one with Dandy-Walker variant.
Güven, M. A., Ceylaner, S. 4th Obstetric, and Gynecological Ultrasonography Congress, Harbiye Military Museum, Istanbul, 6-9 October 2004
55- 2 case reports: It was seen as gross in the ultrasound scan of the 20th week of pregnancy, and at the 38th week of pregnancy.
56- A case with tricuspid atresia; prenatal diagnosis and postnatal assessment.
Güven, M. A., Ceylaner, S., Celasun, B., Beyazıt A. H., Aydemir N. 4th Obstetric and Gynecological Ultrasonography Congress, Harbiye Military Museum, Istanbul, 6-9 October 2004
57- A case report: schisis association- prenatal diagnosis and postmortem evaluation.
Ceylaner, S., Eserdağ, S., Korkmaz, Y., Yuvanç, H. O., Alan, M., Tuğ, M., Mungan, T., Consultant, N. V. Turkish-German Gynecology Association and II. Joint Congress of Reproductive Medicine Controversial Issues and Solutions. Antalya, 16-20 May 2003
58- Prenatal diagnosis of Robinow syndrome.
Eserdağ, S. , Ceylaner, S. , Korkmaz, Y. , Yuvanç, H. O. , Alan, M. , Bayramoğlu, H. , Mungan,T. , Consultant, N V. Turkish-German Gynecology Association, and II. Joint Congress of Reproductive Medicine Controversial Issues and Solutions. Antalya, 16-20 May 2003
59- Prenatal diagnosis of prune belly syndrome.
Consultant, N., Eserdağ, S., Korkmaz, Y., Alan, M., Ceylaner, S., Taner, D., Mungan, T. V. Turkish-German Gynecology Association, and II. Joint Congress of Reproductive Medicine Controversial Issues and Solutions. Antalya, 16-20 May 2003
60- Investigation of sister chromatid exchanges (SCE) in patients with schizophrenia.
Ceylaner, G., Ceylaner, S., Sezgin, I. 3rd National Congress of Prenatal Diagnosis and Medical Genetics, Marmaris, 26-30 April 1998
Genetic evaluation of 61- 93 cases with azoospermia.
Ceylaner, S. , Doğan, M. , Gürbüz, A. S. , Günyeli, İ. , Oral, H. , Küçüközkan, T., X. Infertility and Reproduction congress, Ankara, 26-29 October 2002
62- A syndrome of multiple congenital anomalies (acrocephaly, typical facial appearance, scoliosis, arachnodactyly)
Candemir, Z. , Dundar, M. , Erkılıç, K. , Ceylaner, S. XIII. Gevher Nesibe Medicine Days, Kayseri, 4-7 June 1996
63- A case of ambiguous genitalia with uniparental disomy.
Dundar, M. , Demiryılmaz, F. , Acar, H. , Kurtoğlu, S. , Ceylaner, S. , Küçükaydın, M. XIII. Gevher Nesibe Medicine Days, Kayseri, 4-7 June 1996
64- A family with Duchenne-like muscular dystrophy.
Ceylaner, S. , Özyazgan, I. , Demiryılmaz, F., Dündar, M., Ceylaner, G. , Kandemir, O. IV. Black Sea Medicine Days, Trabzon, 31 May- 3 June 1995
65- Genetic research on tongue movements-III.
Ceylaner, G. , Ceylaner, S. , Akarsu, N. , Şaylı B. S. IV. Black Sea Medicine Days, Trabzon, 31 May- 3 June 1995
66- A case with 22q+ variant ph' chromosomes.
Ceylaner, S. , Cücer, N. , Unal, A. , Özyazgan, I. , Saatçi, Ç. , Ozkul, Y. XII. Gevher Nesibe Medicine Days, Kayseri, 11-14 May 1994
67- Genetic research on tongue movements-II.
Şaylı, B. S. , Ceylaner, S. , Ceylaner, G. II. National Congress of Prenatal Diagnosis and Medical Genetics, Istanbul, 11-13 October 1990
68- Genetic studies on language movements in a part of the normal population.
Şaylı, B. S., Ceylaner, S., Ceylaner, G. National Prenatal Diagnosis and Genetic Structure of Anatolia Symposium, Eskişehir, 1989.
69- Skewed X-inactivation is associated with recurrent spontaneous abortion.
Donations, S.G., Söylemez, F., Cengiz, B., Üstüner, I., Ceylaner, S., Ceylaner, G., Özçelik T., Acar, A. European Human Genetics Conference 2004, Munich, Germany, 12-15 June 2005
70- Prenatal diagnosis of Meckel Gruber Syndrome presenting with renal agenesis: report of a case.
Guven, M. A., Ceylaner, S., Ceylaner, G., Ertas, E. VI. International Congress of the Turkish-German Gynecology Association, Arch Gynecol Obstet (suppl 1), 271, 2005, MFM&P-047, 19-22 May, Antalya, 2005.
71- Prenatal diagnosis of the autosomal recessive type of Robinow syndrome and differential diagnosis.
Guven, M. A., Ceylaner, S., Batukan, C., Ozbek, A., Demirpolat, G., Uzel, M, VI. International Congress of the Turkish-German Gynecology Association, Arch Gynecol Obstet (suppl 1), 271, 2005, MFM&P-048, 19-22 May, Antalya, 2005.
72- A case of fetal anticonvulsant syndrome with severe bilateral upper limb defect.
Guven, M. A., Batukan, C., Ceylaner, S., Ceylaner, G., Uzel, M. International forum on birth, P 20, 8-11 June, Rome, 2005.
73- Trisomy 4 p syndrome: clinical similarities with De Lange syndrome.
Ceylaner, G. , Ceylaner, S. , Consultant, N. , Mollamahmutoğlu, L. European Human Genetics Conference 2005, Prague, Czech Republic, 7-10 May 2005
74- Volume of sampled amniotic fluid and prenatal cytogenetic diagnosis: results of the retrospective study.
Ceylaner, S. , Güven, M. A. , Ceylaner, G. , Gunyeli, I. , Ekerbicer, H. European Human Genetics Conference 2005, Prague, Czech Republic, 7-10 May 2005
75- A study on 85 pregnancies with chromosome abnormality diagnosed cytogenetic analysis.
Gul, D. , Ceylaner, S. , Ceylaner, G. II. World Congress of Perinatal Medicine for Developing Countries, Belek- Antalya/ TURKEY, 1-5 October 2002
76- The results of 863 amniocentesis of Zekai Tahir Burak Hospital.
Ceylaner, G. , Ceylaner, S. , Consultant, N. , Mungan, T. , Yapar, E. G. , Günyeli, İ., Küçüközkan, T. II. World Congress of Perinatal Medicine for Developing Countries, Belek- Antalya/ TURKEY, 1-5 October 2002
77- Congenital anomaly evaluation program in Zekai Tahir Burak Women's Hospital.
Ceylaner, S., Gunyeli, I. , Ekici, E. , Yüksel, B. , Ceylaner, G. , Boylu, M. , Danışman, N. , Tuğ, M. , Küçüközkan, T. II. World Congress of Perinatal Medicine for Developing Countries, Belek- Antalya/ TURKEY 1-5 October 2002
78- The results of postmortem evaluation of 602 fetuses.
Ceylaner, S. , Ceylaner, G. , Consultant, N. , Ekici E. , Günyeli, İ. , Taner D. , Tuğ M. , Küçüközkan, T. II. World Congress of Perinatal Medicine for Developing Countries, Belek- Antalya/ TURKEY 1-5 October 2002
79- Consecutive four twin pregnancies in the same mother.
Seçkin, B., Avşar, F., Ceylaner, S., Gökmen, O. Second World Congress on Controversies in Obstetrics, Gynecology and Infertility, Paris, France, 6-9 September 2001,
80- Genetic assessment of 19 cases of premature ovarian failure.
Ceylaner, G., Ceylaner, S., Moroy, P., Erdemoğlu, E., Gökmen, O. 16th Annual Meeting of the ESHRE Bologna- Italy, 25-28 June 2000
81- Partial trisomy 12q15-q22.
Yılmaz, Z., Erman-Akar, M., Ceylaner, S., Ceylaner, G., Nabaei, S., Gökmen, O. XVI FIGO World Congress of Gynecology and Obstetrics, Washington DC, USA, 3-8 September 2000
82- Cytogenetic research in 298 couples with recurrent spontaneous gestational losses.
Yılmaz, Z., Erman-Akar, M., Yıldız, S., Yuksel, K., Ceylaner, S., Var, T., Gokmen, O. The International Congress on Reproductive Medicine, Obstetrics and Gynecology: Challenges in the Third Millennium, Tel-Aviv Israel, 11-14 April 2000
83- Clinical and cytogenetic assessment of 97 patients with primary amenorrhea.
Yilmaz, Z., Erman-Akar, M., Yıldız, S., Ceylaner, S., Ceylaner, G. The International Congress on Reproductive Medicine, Obstetrics and Gynecology: Challenges in the Third Millenium, Tel-Aviv Israel, 11- April 14, 2000
84- Familial Rokitansky-Kustner-Hauser syndrome (autosomal dominant inheritance?)
Ceylaner, G., Ceylaner, S., Yılmaz, Z., Erman-Akar, M., Yıldız, S The International Congress on Reproductive Medicine, Obstetrics and Gynecology: Challenges in the Third Millenium, Tel-Aviv Israel, 11-14 April 2000
85- Familial aggregation of testicular feminization.
Ceylaner, S. , Ceylaner, G. , Yılmaz, Z. , Yıldız, S. , Erman-Akar, M. The International Congress on Reproductive Medicine, Obstetrics and Gynecology: Challenges in the Third Millenium, Tel-Aviv Israel, 11- April 14, 2000
86- A case with Xp deletion presenting premature ovarian failure and severe scoliosis.
Ceylaner, G. , Ceylaner, S. , Yesilyurt, H. , Yilmaz, Z. , Erman-Akar, M. The International Congress on Reproductive Medicine, Obstetrics and Gynecology: Challenges in the Third Millenium, Tel-Aviv Israel, 11- April 14, 2000
87- Gonadal agenesis associated with Rokitansky syndrome, a report of 3 cases.
Ceylaner, S., Yalcin, H., Yesilyurt, H., Yıldız, S., Yılmaz, Z. The International Congress on Reproductive Medicine, Obstetrics and Gynecology: Challenges in the Third Millenium, Tel-Aviv Israel, 11-14 April, 2000
88- A case presenting findings of both androgen insensitivity syndrome and Marfan syndrome.
Ceylaner, S. , Ceylaner, G. , Aslan, S. , Yesilyurt, H. The International Congress on Reproductive Medicine, Obstetrics and Gynecology: Challenges in the Third Millenium, Tel-Aviv Israel, 11-14 April 2000
89- Increased condensed chromatin amount of T-lymphocyte interphase nuclei of Down syndrome patients.
Demirtaş, H. , Ceylaner, S. , Cücer, N. First European Cytogenetics Conference, Athens, Greece, 22-25 June 1997
90- The effects of the differences in the routine cytogenetics laboratory on the condensed chromatin of the T-lymphocytes.
Ceylaner, S., Demirtaş, H., Ceylaner, G., Cücer, N. British Human Genetics Conference, York 15-17 September 1997
91- An investigation on the differences of condensed chromatin of the T-lymphocyte interphase nuclei among patients with mental retardation.
Ceylaner, S., Ceylaner, G., Cücer, N., Demirtaş, H. British Human Genetics Conference, York 15-17 September 1997
92- A family with osteogenesis imperfecta, frontonasal dysplasia, ear abnormality, and mental retardation.
Ceylaner, G., Ceylaner, S., Dundar, M. British Human Genetics Conference, York 15-17 September 1997
93- A case with multiple pterygium syndrome (Escobar syndrome)
Dundar, M., Ceylaner, S., Ceylaner, G.” British Human Genetics Conference, York 15-17 September 1997
94- The relationship between phytohemagglutinin concentration in the culture medium and condensed chromatin content of human T-lymphocyte interphase nuclei.
Cücer, N. , Demirtaş, H. , Ceylaner, S. 2nd Balkan Meeting On Human Genetics, Istanbul- Turkey
95- Increased sister chromatid exchange (SCE) in Cornelia De Lange syndrome: report of the two cases.
Ceylaner, S. , Ceylaner, G. , Clockmaker, C. 2nd Balkan Meeting On Human Genetics, Istanbul- Türkiye 3-6 September 1996
96- Differences of metaphase rates in acute leukemia cytogenetics: detection by the co-culture method.
Ceylaner, S. , Ceylaner, G. , Ünal, A. , Dündar, M. , Cücer, N. , Patıroğlu, T. 2nd Balkan Meeting On Human Genetics, İstanbul- Turkey 3-6 September 1996
97- A family with X-linked recessive polyarticular juvenile rheumatoid arthritis.
Ceylaner, G. , Ceylaner, S. , İnan, M. , Şaylı, U. , Şaylı B. S. 2nd Balkan Meeting On Human Genetics, İstanbul- Turkey 3-6 September 1996
98- A patient with Mohr syndrome.
Özyazgan, I. , Ceylaner, S. , Dündar, M. , Öztürk, A. , Demiryılmaz, F. , Demirtaş, H. 2nd Balkan Meeting On Human Genetics, İstanbul- Turkey 3-6 September 1996
99- A case with Mullerian duct failure and mature cystic teratoma.
Ceylaner, S. , Demiryılmaz, F. , Dündar, M. , Şahin, Y. , Onursever, A. , Öztürk, F. 2nd Balkan Meeting On Human Genetics, İstanbul- Turkey 3-6 September 1996
100- Familial occurrence of frontonasal dysplasia.
Ceylaner, S., Candemir, Z., Ceylaner, G., Dündar, M. 2nd Balkan Meeting On Human Genetics, Istanbul- Turkey 3-6 September 1996
101- A translocation carrier family and a sib with holoprosencephaly-polydactyly (pseudo trisomy 13) syndrome.
Ceylaner, S. , Ceylaner, G. , Dündar, M. , Özyazgan, I. , Erkılıç, K. , Demiryılmaz, F., Balkanlı, S. 2nd Balkan Meeting On Human Genetics, İstanbul- Turkey 3-6 September 1996
102- A family with multiple single gene mutations and autosomal dominant umbilical hernia.
Ceylaner, S. , Ceylaner, G. , Demiryılmaz, F. , Dündar, M. , Kendirci, M. , Commandş, S. , Özyazgan, I. , Kandemir, O. 2nd Balkan Meeting On Human Genetics, İstanbul- Turkey 3 -6 September 1996
103- Condensed chromatin enhancement in the phytohemagglutinin stimulated lymphocyte interphase nuclei of two xeroderma pigmentosum patients and artificial chromatin condensation of healthy cells by UV irradiation.
Demirtaş, H. , Cücer, N. , Boztosun, N. , Ceylaner, S. , Öztürk, M. 2nd Balkan Meeting On Human Genetics, İstanbul- Turkey 3-6 September 1996
104- Genetic investigations on tongue movements in individuals from a normal population.
Şaylı B. S., Ceylaner, S., Başkaya, G. 8th International Congress of Human Genetics, Washington DC, USA, 6-11 October 1991