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Serdar Ceylaner

Showing results (71-80 of 244) with videos related to

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Molecular Syndromology|April 3, 2025
Phenotypic Delineation of Combined Oxidative Phosphorylation Deficiency-12: Clinical Features of 2 PatientsMeral Bahar Ister, Muge Cinar, Serdar Ceylaner, et al.
Molecular Syndromology|September 26, 2022
Distinct Autism Spectrum Disorder Phenotype and Hand-Flapping Stereotypes: Two Siblings with Novel Homozygous Mutation in <i>TRAPPC9</i> Gene and Literature ReviewHilmi Bolat, Gül Ünsel-Bolat, Hatice Derin, et al.
Prenatal Diagnosis|April 26, 2007
Prenatal diagnosis of a Turkish Bartsocas-Papas syndrome case with upper limb pterigiaGülay Ceylaner, Melih A Güven, Serdar Ceylaner, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|April 29, 2016
Sertoli cell only syndrome with ambiguous genitaliaFatih Gurbuz, Serdar Ceylaner, Seyda Erdogan, et al.
Klinische Padiatrie|August 2, 2024
Non-syndromic Congenital Sodium Diarrhea: A Novel Mutation in the SLC9A3 GeneFerda Ozbay Hosnut, Gulseren Sahin, Bulent Uyanik, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|January 1, 2026
A novel FGG variant associated with hereditary hepatic fibrinogen storage disease from AdanaAbdul Samet Ala, Talip Sayar, Serdar Ceylaner, et al.
Platelets|May 5, 2025
A case with a novel GATA1 variant mimicking immune thrombocytopenia attacksElif Habibe Aktekin, Serdar Ceylaner, Şeyda Beşen, et al.
Journal of Bone Oncology|December 21, 2018
Association of vitamin D receptor gene polymorphisms with osteosarcoma risk and prognosisNilgun Kurucu, Gurses Şahin, Neriman Sarı, et al.
American Journal of Obstetrics and Gynecology|September 30, 2008
Y chromosome azoospermia factor region microdeletions and recurrent pregnancy lossAbdullah Karaer, Kadri Karaer, Gulnur Ozaksit, et al.
American Journal of Medical Genetics. Part A|June 18, 2009
A boy with trisomy 13 presenting with a subtle clinical picture and metopic synostosisSevim Unal, Fatma Cakmak Celik, Derya Soy, et al.
Pageof 25

Showing results (71-80 of 244) with videos related to

Sort By:
Pageof 25
Molecular Syndromology|April 3, 2025
Phenotypic Delineation of Combined Oxidative Phosphorylation Deficiency-12: Clinical Features of 2 PatientsMeral Bahar Ister, Muge Cinar, Serdar Ceylaner, et al.
Molecular Syndromology|September 26, 2022
Distinct Autism Spectrum Disorder Phenotype and Hand-Flapping Stereotypes: Two Siblings with Novel Homozygous Mutation in <i>TRAPPC9</i> Gene and Literature ReviewHilmi Bolat, Gül Ünsel-Bolat, Hatice Derin, et al.
Prenatal Diagnosis|April 26, 2007
Prenatal diagnosis of a Turkish Bartsocas-Papas syndrome case with upper limb pterigiaGülay Ceylaner, Melih A Güven, Serdar Ceylaner, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|April 29, 2016
Sertoli cell only syndrome with ambiguous genitaliaFatih Gurbuz, Serdar Ceylaner, Seyda Erdogan, et al.
Klinische Padiatrie|August 2, 2024
Non-syndromic Congenital Sodium Diarrhea: A Novel Mutation in the SLC9A3 GeneFerda Ozbay Hosnut, Gulseren Sahin, Bulent Uyanik, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|January 1, 2026
A novel FGG variant associated with hereditary hepatic fibrinogen storage disease from AdanaAbdul Samet Ala, Talip Sayar, Serdar Ceylaner, et al.
Platelets|May 5, 2025
A case with a novel GATA1 variant mimicking immune thrombocytopenia attacksElif Habibe Aktekin, Serdar Ceylaner, Şeyda Beşen, et al.
Journal of Bone Oncology|December 21, 2018
Association of vitamin D receptor gene polymorphisms with osteosarcoma risk and prognosisNilgun Kurucu, Gurses Şahin, Neriman Sarı, et al.
American Journal of Obstetrics and Gynecology|September 30, 2008
Y chromosome azoospermia factor region microdeletions and recurrent pregnancy lossAbdullah Karaer, Kadri Karaer, Gulnur Ozaksit, et al.
American Journal of Medical Genetics. Part A|June 18, 2009
A boy with trisomy 13 presenting with a subtle clinical picture and metopic synostosisSevim Unal, Fatma Cakmak Celik, Derya Soy, et al.
Pageof 25