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Genetic Counseling (Geneva, Switzerland)|April 30, 2009
Frontonasal dysplasia: a family presenting autosomal dominant inheritance patternH Koçak, G CeylanerGenetic Counseling (Geneva, Switzerland)|November 11, 2008
Azoospermia and cryptorchidism in a male with a de novo reciprocal t(Y;16) translocationM Gunel, S Cavkaytar, G Ceylaner, et al.Genetic Counseling (Geneva, Switzerland)|February 21, 2014
Ring chromosome 9 in a newbornO Aldemir, I H Celik, K Karaer, et al.Genetic Counseling (Geneva, Switzerland)|August 5, 2009
Prenatal diagnosis of a case with anencephaly-omphalocele-unilateral absent radial rayS Ceylaner, G Ceylaner, M Altun, et al.Genetic Counseling (Geneva, Switzerland)|December 18, 2013
Prenatal diagnosis of Goldenhar syndrome with unusual features by 3D ultrasonographyI Guzelmansur, G Ceylaner, S Ceylaner, et al.Genetic Counseling (Geneva, Switzerland)|August 19, 2011
Ovulation induction with gonadotropins causes increased sister chromatid exchangesE Tonguç, G Ceylaner, T Var, et al.Genetic Counseling (Geneva, Switzerland)|August 5, 2009
Prenatal diagnosis of a case probably with Oral-Facial-Digital Syndrome--Gabrielli typeM A Güven, G Ceylaner, S Ceylaner, et al.Genetic Counseling (Geneva, Switzerland)|February 26, 2009
A prenatally diagnosed case of sirenomelia with polydactyly and vestigial tailM A Guven, M Uzel, S Ceylaner, et al.Genetic Counseling (Geneva, Switzerland)|April 28, 2010
Partial trisomy due to a de novo duplication 22q11.1-22q13.1: a cat-eye syndrome variant with brain anomaliesD Karcaaltincaba, S Ceylaner, G Ceylaner, et al.Genetic Counseling (Geneva, Switzerland)|May 28, 2011
A novel mutation in the RPS6KA3 gene in a patient with Coffin-Lowry syndromeS Senel, S Ceylaner, G Ceylaner, et al.Pageof 2