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 (11-20 of 29) with videos related to

Pageof 3
Sort By:
Genetic Counseling (Geneva, Switzerland)|February 5, 2011
A case of lower mesodermal defects sequenceT Tos, S Aktas, M Ikbal, et al.
Genetic Counseling (Geneva, Switzerland)|May 25, 2006
Prenatal diagnosis of Meckel Gruber syndrome presenting with renal agenesis: report of a caseM A Guven, S Ceylaner, G Ceylaner, et al.
Genetic Counseling (Geneva, Switzerland)|February 9, 2016
REVERSIBLE CLINICAL AND MAGNETIC RESONANCE IMAGING FINDINGS IN LATE-ONSET COBALAMIN C DEFECTE Gurkas, A Kartal, K Aydin, et al.
Balkan Journal of Medical Genetics : BJMG|March 14, 2024
Do Gene Polymorphisms Play a Role in Newborn Hyperbilirubinemia?N Hakan, M Aydin, S Ceylaner, et al.
Clinical Pediatrics|August 9, 2001
Cutis laxa with growth and developmental delayC Karakurt, T Sipahi, S Ceylaner, et al.
Balkan Journal of Medical Genetics : BJMG|August 14, 2023
Difficulties in Diagnosing Fabry Disease in Patients with Unexplained Left Ventricular Hypertrophy (LVH): Is the Novel GLA Gene Mutation a Pathogenic Mutation or Polymorphism?N Aladağ, H Ali Barman, A Şipal, 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.
Journal of Medical Genetics|June 1, 1995
A large Turkish kindred with syndactyly type II (synpolydactyly). 1. Field investigation, clinical and pedigree dataB S Sayli, A N Akarsu, U Sayli, et al.
Pageof 3

Showing results (11-20 of 29) with videos related to

Sort By:
Pageof 3
Genetic Counseling (Geneva, Switzerland)|February 5, 2011
A case of lower mesodermal defects sequenceT Tos, S Aktas, M Ikbal, et al.
Genetic Counseling (Geneva, Switzerland)|May 25, 2006
Prenatal diagnosis of Meckel Gruber syndrome presenting with renal agenesis: report of a caseM A Guven, S Ceylaner, G Ceylaner, et al.
Genetic Counseling (Geneva, Switzerland)|February 9, 2016
REVERSIBLE CLINICAL AND MAGNETIC RESONANCE IMAGING FINDINGS IN LATE-ONSET COBALAMIN C DEFECTE Gurkas, A Kartal, K Aydin, et al.
Balkan Journal of Medical Genetics : BJMG|March 14, 2024
Do Gene Polymorphisms Play a Role in Newborn Hyperbilirubinemia?N Hakan, M Aydin, S Ceylaner, et al.
Clinical Pediatrics|August 9, 2001
Cutis laxa with growth and developmental delayC Karakurt, T Sipahi, S Ceylaner, et al.
Balkan Journal of Medical Genetics : BJMG|August 14, 2023
Difficulties in Diagnosing Fabry Disease in Patients with Unexplained Left Ventricular Hypertrophy (LVH): Is the Novel GLA Gene Mutation a Pathogenic Mutation or Polymorphism?N Aladağ, H Ali Barman, A Şipal, 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.
Journal of Medical Genetics|June 1, 1995
A large Turkish kindred with syndactyly type II (synpolydactyly). 1. Field investigation, clinical and pedigree dataB S Sayli, A N Akarsu, U Sayli, et al.
Pageof 3