Courses, Congresses, Conferences, and Training
Intergen continues its activities towards the dissemination of scientific activities with the courses, congresses, conferences, and training it organizes.
1- Mediterranean fever (MEVF) gene mutations in Behçet patients with and without ocular involvement.
Nilüfer Yalçındağ, Yeşim Gedik-Oğuz, Serdar Ceylaner 12th INTERNATIONAL OCULAR INFLAMMATION SOCIETY CONGRESS 2nd INTERNATIONAL ASSEMBLY OF OCULAR INFLAMMATION SOCIETIES 27th SPANISH UVEITIS STUDY GROUP MEETING February 27th-28th and March 1st
2- Self-mutilation and kidney stones: Two case reports with partial and complete Lesch-Nyhan Syndrome
Neslihan Önenli Mungan, Deniz Kör, Aysun Karabay Beyazıt, Serdar Ceylaner, Sevcan Erdem, Faruk İncecik, Ali Anarat Türk Ped Arş 2013 Special Issue; 16-172
3- A case of Smith-LemliOpitz Syndrome diagnosed with dysmorphic findings in the early period
İlyas Okur, Mehmet Gündüz, Fatma Güzel, Nevra Koç, Fevziye Chairman Vuralkan, Serdar Ceylaner Türk Ped Arş 2013 Special Issue; 16-172
4- TAR syndrome diagnosis confirmed by aCGH analysis.
S. Ceylaner, Y. K. Terzi, S. Kalyoncu, F. I. Sahin. The ASHG Annual Meeting in San Francisco, California from Tuesday, November 6 through Saturday, November 10, 2012
5- Are endothelial nitric oxide synthase gene 894 g>t and 786 t>c polymorphıisms risk factors for endometriosis?
Ayranci, H.; Dogan, H.; Ceylaner, S. XX FIGO World Congress of Gynecology and Obstetrics, International Journal of Gynecology and Obstetrics October 2012 119 Supplement 3:S327-S328
6- “Journal of Clinical Research in Pediatric Endocrinology”, 2011 best case report award - Sporadic Nonautoimmune Neonatal Hyperthyroidism Due to A623V Germline Mutation in the Thyrotropin Receptor Gene.
Aycan Z, Ceylaner S, Yılmaz Ağdıoğlu S, Çetinkaya S, Chief VN, Peltek Kendirci HN
7- Cleft palate in a patient with the 9p deletion syndrome,
Far, Asli Subasioglu; Ceylaner, Serdar; Erdogan, Murat; Karabulut, Yesim; Balta, Burhan; Bahadir, Oguzhan; Kurt, Fatima; Dogan, Muhammed; Dundar, Munis In European Biotechnology Congress 2011, Current Opinion in Biotechnology 2011 22 Supplement 1:S106
8- The Relationship Between Nuchal Edema, Cystic Hygroma and Non-Immune Hydrops Causing Fetal Subcutaneous Edema and Chromosomal Anomalies
D.C. Arıkan, A. Coskun, G. Kıran, H. Kıran, M.A. Güven, S., Turkish Maternal Fetal Medicine and Perinatology Society 7th National Congress 122 pp., Istanbul, Turkey, September 2010.
9- The major cause of terminal transverse limb defect and related syndromes is thrombophilia. The results of the prospective study.
S. Ceylaner, G. Ceylaner, Acar K., Gul D., Zencirlioğlu A., Okumuş N. 9th National Medical Genetic Congress of Turkish Medical Society with International Participation. Istanbul, 1-5 Dec 2010. Clinical Genetics 2010 78 (1)
10- Disorders of contiguous genes are not always “Contiguous gene syndrome”: Lessons from a case with three different genetic disorders.
Aslan D., G. Ceylaner., S. Ceylaner. 9th National Medical Genetic Congress of Turkish Medical Society with International Participation. Istanbul, 1-5 Dec 2010. Clinical Genetics 2010 78 (1)
11- Amniotic fluid cell culture and syringe toxicity.
G. Ceylaner., M.A. Güven, S. Ceylaner., Ekerbiçer H. 9th National Medical Genetic Congress of Turkish Medical Society with International Participation. Istanbul, 1-5 Dec 2010. Clinical Genetics 2010 78 (1)
12- Osteogenesis imperfecta type 2 prenatal 2b, 3b US and postnatal 3b CT findings.
Güzelmansur İ., Şahin E., Ceylan N., G. Ceylaner. 30th National Radiology Congress Antalya, 04-09 November 2009
13- Radial ray malformation. 2b, 3b US and postnatal 3d CT findings.
Güzelmansur İ., Şahin E., Ceylan N., G. Ceylaner. 30th National Radiology Congress Antalya, 04-09 November 2009
14- Is QF-PCR or FISH method sufficient in prenatal diagnosis? Analysis of 417 cases with chromosomal irregularity in amniotic fluid.
Gül D., S. Ceylaner., G. Ceylaner. 12. National Perinatology Congress, Antalya, 23-26 April 2009
15- Analysis of 163 pregnancy evacuation materials with chromosome irregularity.
Gül D., S. Ceylaner., G. Ceylaner. 12. National Perinatology Congress, Antalya, 23-26 April 2009
16- Prenatal diagnosis of trisomy 3: A case report.
Arıkan D.C., Coşkun A., Kıran G., G. Ceylaner. 12. National Perinatology Congress, Antalya, 23-26 April 2009
17- The most common cause of terminal transverse limb defects is thrombophilia. Prospective study results.
G. Ceylaner., S. Ceylaner., Acar K., Gül D., Zencirlioğlu A., Okumuş N. 7th National Pediatric Hematology Congress, Ankara, 24-27 May 2009
18- Contribution of genetic approach and new methods in pediatric hematological cancers.
S. Ceylaner., G. Ceylaner., Gül D. 7th National Pediatric Hematology Congress, Ankara, 24-27 May 2009
19- Osteogenesis imperfecta type 2 prenatal 2b, 3b US and postnatal 3b CT findings.
Güzelmansur İ., Şahin E., Ceylan N., G. Ceylaner. 30th National Radiology Congress Antalya, 04-09 November 2009
20- Radial ray malformation. 2b, 3b US and postnatal 3d CT findings.
Güzelmansur İ., Şahin E., Ceylan N., G. Ceylaner. 30th National Radiology Congress Antalya, 04-09 November 2009
21- Thrombophilia is the most common cause of terminal transverse limb defects: results of a prospective study
Gülay Ceylaner, Serdar Ceylaner, Kadir Acar, Davut Gül, Ayşegül Zencirlioğlu, Nurullah Okumuş 7th National Pediatric Hematology Congress 24-27 May 2009 Ankara
22- Contribution of general genetic approach and new methods in pediatric hematological cancers
Serdar Ceylaner, Gülay Ceylaner, Davut Gül 7th National Pediatric Hematology Congress 24-27 May 2009 Ankara
23- Neu-Laxova Syndrome: A case report.
Mutlu B, Narlı N, Özcan K, Ceylaner S, Yıldıztaş H, Satar M. 17th National Neonatology Congress, 27-30 April 2009, Çeşme, İzmir page 224.
24- Retrospective Evaluation of Amniocentesis Cases
Coskun, D. C. Arıkan, G. Kıran, M. A. Güven, B. Köstü, S. Ceylaner, 12th National Perinatology Congress 30 pp., Antalya, Turkey, April 2009
25- Investigating Factor V (G1691A), Prothrombin (G20210A), and Methylenetetrahydrofolate reductase (C677T) gene polymorphisms in recurrent pregnancy loss
European Human Genetics Conference, 31 May-3 June 2008., , 2008(with Samli H. , Imirzalioglu N., Koken G., Ceylaner G. , Ceylaner S. ,)
26- Pycnodysostosis Associated with Mitral Valve Prolapse: A Case Report of Two Siblings
Esma Altınel, Aysel Yöney, Saliha Şenel, Nilgün Erkek, Candemir Karacan, Utku Arman Örün, Serdar Ceylaner 4th ULUDAĞ PEDIATRIC WINTER CONGRESS 18-19 March 2008
27- Güven E.S.G, Ceylaner S, Çınar Ö, Dilbaz S, Aydın S, Gürsoy S, Haberal A. 46, XY, İ (9) (P10), İ (9) (Q10) Karyotype Anomaly in Man with Oligoasthenoteratozoospermia Reversible with Treatment. 3. National Reproductive Endocrinology and Infertility Congress, Antalya, 16-19.10.2008.
28- A case with Rubinstein-Taybi syndrome.
Kuraş Can Y, Erdoğan F., Ceylaner S, Çelik A, Özdemir O, Yılmaz G. 51st National Pediatrics Congress 2007
29- Prenatal diagnosis of theophoric dysplasia type I: ultrasonographic and biochemical findings
Erdemoglu, E., T. Mungan, S. Ceylaner and M. Tezimer, 31. Advanced course on ultrasound in obstetrics and gynecology, 19.20 May, Antalya. Ultrasonography Obstetrics and Gynecology 6(1-2), S56
30- The role of hereditary thrombophilic factors in deep venous thrombosis
Bardakcı, H., G. Ceylaner, S. Ceylaner, Kervan, Ü., Tuncel, Ç., Birincioglu, L. 13. National Vascular Surgery Congress, 22-26 May, 2007
31- 12+3. Trisomy 18 case presenting with increased NT at the gestational week and accompanied by the diagnosis of DORV, VSD
Güven, M. A., G. S. Ceylaner Ceylaner, A. Coskun, P-55, 5th Congress of Obstetrics and Gynecology Ultrasound, Antalya, 2006
32- A case of Pentalogy of Cantrell diagnosed prenatally
Güven, M. A., G. S. Ceylaner Ceylaner, A. Coskun, P-54, 5th Congress of Obstetrics and Gynecology Ultrasound, Antalya, 2006
33- A case of Campomelic Dysplasia diagnosed prenatally
Güven, M. A., G. S. Ceylaner Ceylaner, A. Coskun, P-53, 5th Congress of Obstetrics and Gynecology Ultrasound, Antalya, 2006
34- Lethal multiple pterygium syndrome with standing ectrodactyly
G. Ceylaner, M. A. Güven, S. Ceylaner, A. Coskun P-51, 5th Congress of Obstetrics and Gynecology Ultrasound, Antalya, 2006
35- Bartsocas-Papas syndrome was diagnosed prenatally and presented with upper extremity pterygia
G. Ceylaner, M. A. Güven, S. Ceylaner, A. Coskun, P-52, 5th Congress of Obstetrics and Gynecology Ultrasound, Antalya, 2006
36- Prenatal diagnosis and postmortem evaluation results.
S. Ceylaner., Eserdağ S, G. Ceylaner., Supervisor N. Michould VII. National Congress of Prenatal Diagnosis and Medical Genetics. Kayseri, 17-20 May 2006
37- Identical twins with signs of hypogonadism.
G. Ceylaner., Aktürk M., Şahin İ, S. Ceylaner., Mollamahmutoğlu L. Alopecia, VII. National Congress of Prenatal Diagnosis and Medical Genetics. Kayseri, 17-20 May 2006
38- Autosomal recessive imperforate hymen.
G. Ceylaner., S. Ceylaner., Akın Su F., Mollamahmutoğlu L. VII. National Congress of Prenatal Diagnosis and Medical Genetics. Kayseri, 17-20 May 2006
39- Prenatal diagnosis of a case with EMANUEL syndrome (supernumerary der (22) syndrome)
M. A. Guven, G. Ceylaner, S. Ceylaner, A. Coskun 16th World Congress on Ultrasound in Obstetrics and Gynecology, 3-7 September 2006, London, UK.
40- Prenatal diagnosis of Mohr syndrome
M. A. Guven, G. Ceylaner2, S. Ceylaner, M. Uzel, A. Coskun 16th World Congress on Ultrasound in Obstetrics and Gynecology, 3-7 September 2006, London, UK.
41- A prenatally diagnosed and postnatally confirmed case of with Saldino-Noonan syndrome
M.A. Guven, S. Ceylaner, M. Uzel, A. Coskun, G. Ceylaner, XX European Congress of Perinatal and Neonatal Medicine, P-03-003, 24-27 May, Prague, 2006
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