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S Ceylaner

Showing results (21-30 of 29) with videos related to

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Genetic Counseling (Geneva, Switzerland)|February 28, 2018
Kept in Mind Infantile Neuroaxonal DystrophyZ S Karalok, B D Taskin, U Aydogmus, et al.
Genetic Counseling (Geneva, Switzerland)|September 15, 2006
An infant with diaphragmatic hernia, anophthalmia and cardiac defect: evaluation by magnetic resonance imaging autopsyS Ceylaner, H E Gozer, G Ceylaner, et al.
Genetic Counseling (Geneva, Switzerland)|October 27, 2009
A Feingold syndrome case with previously undescribed features and a new mutationH Koçak, E Ozaydin, G Köse, et al.
Genetic Counseling (Geneva, Switzerland)|July 16, 2008
Goldenhar syndrome associated with growth hormone deficiencyA M Yusufoğlu, E Cetinkaya, S Ceylaner, et al.
Journal of Obstetrics and Gynaecology : the Journal of the Institute of Obstetrics and Gynaecology|June 6, 2012
Carbamazepine use in pregnancy and coincidental thalidomide-like phocomelia in a newbornA Dursun, N Karadağ, B Karagöl, et al.
Genetic Counseling (Geneva, Switzerland)|February 9, 2016
CITRIN DEFICIENCY: AN INFANT INCIDENTALLY DETECTED BY PHENYLKETONURIA SCREENING WITH A NOVEL MUTATION IN SLC25A13 GENEA C Aktuglu Zeybek, E Kiykim, T Zubarioglu, et al.
Genetic Counseling (Geneva, Switzerland)|August 11, 2012
A new family with autosomal dominant porencephaly with a novel Col4A1 mutation. Are arachnoid cysts related to Col4A1 mutations?A Değerliyurt, G Ceylaner, H Koçak, et al.
Transplantation Proceedings|April 30, 2013
Nephron-sparing surgery for renal cell carcinoma of the allograft after renal transplantation: report of two casesA Tuzuner, F Çakir, C Akyol, et al.
Clinical Genetics|January 4, 2012
High frequency of p.Thr93Met in Smith-Lemli-Opitz syndrome patients in TurkeyS Kalb, A O Caglayan, A Degerliyurt, et al.
Pageof 3

Showing results (21-30 of 29) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 29 results.
Genetic Counseling (Geneva, Switzerland)|February 28, 2018
Kept in Mind Infantile Neuroaxonal DystrophyZ S Karalok, B D Taskin, U Aydogmus, et al.
Genetic Counseling (Geneva, Switzerland)|September 15, 2006
An infant with diaphragmatic hernia, anophthalmia and cardiac defect: evaluation by magnetic resonance imaging autopsyS Ceylaner, H E Gozer, G Ceylaner, et al.
Genetic Counseling (Geneva, Switzerland)|October 27, 2009
A Feingold syndrome case with previously undescribed features and a new mutationH Koçak, E Ozaydin, G Köse, et al.
Genetic Counseling (Geneva, Switzerland)|July 16, 2008
Goldenhar syndrome associated with growth hormone deficiencyA M Yusufoğlu, E Cetinkaya, S Ceylaner, et al.
Journal of Obstetrics and Gynaecology : the Journal of the Institute of Obstetrics and Gynaecology|June 6, 2012
Carbamazepine use in pregnancy and coincidental thalidomide-like phocomelia in a newbornA Dursun, N Karadağ, B Karagöl, et al.
Genetic Counseling (Geneva, Switzerland)|February 9, 2016
CITRIN DEFICIENCY: AN INFANT INCIDENTALLY DETECTED BY PHENYLKETONURIA SCREENING WITH A NOVEL MUTATION IN SLC25A13 GENEA C Aktuglu Zeybek, E Kiykim, T Zubarioglu, et al.
Genetic Counseling (Geneva, Switzerland)|August 11, 2012
A new family with autosomal dominant porencephaly with a novel Col4A1 mutation. Are arachnoid cysts related to Col4A1 mutations?A Değerliyurt, G Ceylaner, H Koçak, et al.
Transplantation Proceedings|April 30, 2013
Nephron-sparing surgery for renal cell carcinoma of the allograft after renal transplantation: report of two casesA Tuzuner, F Çakir, C Akyol, et al.
Clinical Genetics|January 4, 2012
High frequency of p.Thr93Met in Smith-Lemli-Opitz syndrome patients in TurkeyS Kalb, A O Caglayan, A Degerliyurt, et al.
Pageof 3