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Gülay Ceylaner

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Physiology

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TOP 3
Acar Tuzuner; Sule Sengül; Cihangir Akyol; F Cakir; Z K Celebi; Gülay Ceylaner; Serdar Ceylaner; Kenan Keven
Nephron-sparing Surgery for Renal Cell Carcinoma of the Allograft After Renal Transplantation: Report of Two Cases.
S Kalb; S Kurtoglu; H Rehder; S Schmid; A O Caglayan; Gülay Ceylaner; S Ceylaner; A Degerliyurt; N Hatipoglu; K Hinderhofer; J Zschocke; M Witsch-Baumgartner
High frequency of p.Thr93Met in Smith-Lemli-Opitz syndrome patients in Turkey.
A Değerliyurt; H Koçak; P Rizzu; B Bilginer Gürbüz; Gülay Ceylaner; B S Cihan; Serdar Ceylaner
A new family with autosomal dominant porencephaly with a novel Col4A1 mutation. Are arachnoid cysts related to Col4A1 mutations?

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2013: Acar Tuzuner; Sule Sengül; Cihangir Akyol; F Cakir; Z K Celebi; Gülay Ceylaner; Serdar Ceylaner; Kenan Keven
Nephron-sparing Surgery for Renal Cell Carcinoma of the Allograft After Renal Transplantation: Report of Two Cases.
Transplantation proceedings 2013;45(3):958-60.
2012: S Kalb; S Kurtoglu; H Rehder; S Schmid; A O Caglayan; Gülay Ceylaner; S Ceylaner; A Degerliyurt; N Hatipoglu; K Hinderhofer; J Zschocke; M Witsch-Baumgartner
High frequency of p.Thr93Met in Smith-Lemli-Opitz syndrome patients in Turkey.
Clinical genetics 2012;81(6):598-601.
2012: A Değerliyurt; H Koçak; P Rizzu; B Bilginer Gürbüz; Gülay Ceylaner; B S Cihan; Serdar Ceylaner
A new family with autosomal dominant porencephaly with a novel Col4A1 mutation. Are arachnoid cysts related to Col4A1 mutations?
Genetic counseling (Geneva, Switzerland) 2012;23(2):185-93.
2011: E Tonguç; T Var; E Zülfkaroğlu; Gülay Ceylaner; Serdar Ceylaner
Ovulation induction with gonadotropins causes increased sister chromatid exchanges.
Genetic counseling (Geneva, Switzerland) 2011;22(2):193-8.
2008: Melih Atahan GUVEN; M Uzel; Serdar Ceylaner; A Coskun; Gülay Ceylaner; A Gungoren
A prenatally diagnosed case of sirenomelia with polydactyly and vestigial tail.
Genetic counseling (Geneva, Switzerland) 2008;19(4):419-24.
2007: Gülay Ceylaner; Serdar Ceylaner; Nuri Danişman; Ali Ergün; Eyüp Ekici; Albert Schinzel; Alessandra Baumer
Chromosomal heteromorphisms may help for the diagnosis of uniparental disomy (UPD): a case report.
Prenatal diagnosis 2007;27(11):1072-4.
2007: Gülay Ceylaner; Serdar Ceylaner; Ilker Günyeli; Eyüp Ekici; Bülent Celasun; Nuri Danişman
Evaluation of 2407 fetuses in a Turkish population.
Prenatal diagnosis 2007;27(9):800-7.
2007: Gülay Ceylaner; Melih A Güven; Serdar Ceylaner; Murat Uzel; Kamil Müftüoğlu
Prenatal diagnosis of a Turkish Bartsocas-Papas syndrome case with upper limb pterigia.
Prenatal diagnosis 2007;27(6):563-5.
2006: Melih Atahan GUVEN; Gülay Ceylaner; A Coskun
Volume of sampled amniotic fluid and prenatal cytogenetic diagnosis.
International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics 2006;95(2):157-8.
2006: Sevgi Bagislar; Isik Ustuner; Bora Cengiz; Feride Soylemez; Cemaliye Boylu Akyerli; Serdar Ceylaner; Gülay Ceylaner; Aynur Acar; Tayfun Ozcelik
Extremely skewed X-chromosome inactivation patterns in women with recurrent spontaneous abortion.
The Australian & New Zealand journal of obstetrics & gynaecology 2006;46(5):384-7.
2006: Melih Atahan GUVEN; Cem Batukan; Serdar Ceylaner; Gülay Ceylaner; Murat Uzel
A case of fetal anticonvulsant syndrome with severe bilateral upper limb defect.
The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians 2006;19(2):115-7.
2006: Serdar Ceylaner; Gülay Ceylaner; Ilker Günyeli; Eyüp Ekici; Mengü Tuğ; Dilara Taner; Hasan Ekerbicer; Leyla Mollamahmutoğlu; Nuri Danişman
Postmortem evaluation of 220 prenatally diagnosed fetuses with neural tube defects: detection of associated anomalies in a Turkish population.
Prenatal diagnosis 2006;26(2):147-53.
2006: Serdar Ceylaner; H E Gozer; Gülay Ceylaner; Ibrahim Egemen Ertas; S U Kizilates; T Edguer
An infant with diaphragmatic hernia, anophthalmia and cardiac defect: evaluation by magnetic resonance imaging autopsy.
Genetic counseling (Geneva, Switzerland) 2006;17(2):231-6.
2006: M A Guven; Serdar Ceylaner; Gülay Ceylaner; D Gul; Ibrahim Egemen Ertas
Prenatal diagnosis of Meckel Gruber syndrome presenting with renal agenesis: report of a case.
Genetic counseling (Geneva, Switzerland) 2006;17(1):65-8.
2005: Linda C Walker; Mayra A Overstreet; Adnan Siddiqui; Anne De Paepe; Gülay Ceylaner; Fransiska Malfait; Sofie Symoens; Phimon Atsawasuwan; Mitsuo Yamauchi; Serdar Ceylaner; Ruud A Bank; Heather N Yeowell
A novel mutation in the lysyl hydroxylase 1 gene causes decreased lysyl hydroxylase activity in an Ehlers-Danlos VIA patient.
The Journal of investigative dermatology 2005;124(5):914-8.
2005: Dilek Güven; Serdar Ceylaner; Defne Kalayci; Gülay Ceylaner; Hikmet Hasiripi
Craniosynostosis and ectopia lentis in a propositus whose parents are cousins.
American journal of medical genetics. Part A 2005;134A(2):231.