Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

S Ceylaner

Showing results (1-10 of 29) with videos related to

Pageof 3
Sort By:
Genetic Counseling (Geneva, Switzerland)|August 11, 2012
A 7q11.23 microduplication patient with cerebral palsy and facial dysmorphismA Değerliyurt, S Ceylaner, H Ozdağ
Genetic Counseling (Geneva, Switzerland)|April 25, 2013
Acromesomelic dysplasia with cardiac and neurologic abnormalities: an association by chance, new features of maroteaux type or a new syndrome?F Kurt, S Ceylaner, H I Yakut
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)|March 26, 2015
Single median maxillary central incisor syndrome and its clinical importanceH Aydemir, S Aydemir, T Bezgin, 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)|October 23, 2010
A case of otocephaly with anencephaly and meningomyeloceleT Tos, S Ceylaner, S Senel, et al.
Genetic Counseling (Geneva, Switzerland)|June 6, 2015
A familial case of Coffin-Lowry syndrome caused by RPS6KA3 C.898C>T mutation associated with multiple abnormal brain imaging findingsT Tos, M Y Alp, A Aksoy, et al.
Genetic Counseling (Geneva, Switzerland)|July 16, 2008
Apparent Lenz microphthalmia syndrome: a patient with unusual manifestationsN Okumus, A Zenciroglu, N Demirel, 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.
Pageof 3

Showing results (1-10 of 29) with videos related to

Sort By:
Pageof 3
Genetic Counseling (Geneva, Switzerland)|August 11, 2012
A 7q11.23 microduplication patient with cerebral palsy and facial dysmorphismA Değerliyurt, S Ceylaner, H Ozdağ
Genetic Counseling (Geneva, Switzerland)|April 25, 2013
Acromesomelic dysplasia with cardiac and neurologic abnormalities: an association by chance, new features of maroteaux type or a new syndrome?F Kurt, S Ceylaner, H I Yakut
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)|March 26, 2015
Single median maxillary central incisor syndrome and its clinical importanceH Aydemir, S Aydemir, T Bezgin, 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)|October 23, 2010
A case of otocephaly with anencephaly and meningomyeloceleT Tos, S Ceylaner, S Senel, et al.
Genetic Counseling (Geneva, Switzerland)|June 6, 2015
A familial case of Coffin-Lowry syndrome caused by RPS6KA3 C.898C>T mutation associated with multiple abnormal brain imaging findingsT Tos, M Y Alp, A Aksoy, et al.
Genetic Counseling (Geneva, Switzerland)|July 16, 2008
Apparent Lenz microphthalmia syndrome: a patient with unusual manifestationsN Okumus, A Zenciroglu, N Demirel, 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.
Pageof 3