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Serdar Ceylaner

Showing results (31-40 of 244) with videos related to

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Clinical Neurology and Neurosurgery|January 26, 2021
A newborn case of adenylosuccinate lyase deficiency with a novel heterozygous mutation diagnosed by whole exome sequencingFatma Cakmak Celik, Mehmet Mustafa Ozlu, Serdar Ceylaner
Endocrine, Metabolic & Immune Disorders Drug Targets|November 14, 2022
Renal Involvement in H Syndrome, A Rare Cause of Diabetes Mellitus: Case ReportRecep Polat, Ala Ustyol, Rabia Altunbaş, et al.
Turkish Journal of Haematology : Official Journal of Turkish Society of Haematology|July 31, 2023
Hb Andrew-Minneapolis Variant in a Turkish FamilyHamza Sümter, Soycan Mızrak, Serdar Ceylaner, et al.
The Turkish Journal of Pediatrics|July 24, 2018
Microcephaly and developmental delay caused by short-chain acyl-CoA dehydrogenase deficiencyMustafa Kılıç, Saliha Şenel, Kadri Karaer, et al.
Acta Orthopaedica Et Traumatologica Turcica|December 9, 2008
[Autosomal dominant inheritance of congenital dislocation of the hip in 16 members of a family]Gülay Ceylaner, Serdar Ceylaner, Fulya Ustünkan, et al.
International Journal of Gynaecology and Obstetrics: the Official Organ of the International Federation of Gynaecology and Obstetrics|May 18, 2010
Genetic abnormalities in Turkish women with premature ovarian failureGulay Ceylaner, Sunduz Ozlem Altinkaya, Leyla Mollamahmutoglu, et al.
Journal of Clinical Research in Pediatric Endocrinology|August 12, 2021
Compound Heterozygous Variants in <i>FAM111A</i> Cause Autosomal Recessive Kenny-Caffey Syndrome Type 2Erdal Eren, Havva Tezcan Ünlü, Serdar Ceylaner, et al.
Case Reports in Immunology|July 14, 2022
A Case of Common Variable Immunodeficiency with CREBP Gene Mutation without Rubinstein Taybi Syndrome FeaturesUgur Musabak, Serdar Ceylaner, Tuba Erdogan, et al.
Molecular Reproduction and Development|August 31, 2002
Evaluation of segregation patterns of 21;21 Robertsonian translocation along with sex chromosomes and interchromosomal effects in sperm nuclei of carrier by FISH techniqueHasan Acar, M Selman Yildirim, Tülin Cora, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|August 10, 2011
A new variant of a known mutation in two siblings with permanent neonatal diabetes mellitusZehra Aycan, Semra Cetinkaya, Serife Suna Oğuz, et al.
Pageof 25

Showing results (31-40 of 244) with videos related to

Sort By:
Pageof 25
Clinical Neurology and Neurosurgery|January 26, 2021
A newborn case of adenylosuccinate lyase deficiency with a novel heterozygous mutation diagnosed by whole exome sequencingFatma Cakmak Celik, Mehmet Mustafa Ozlu, Serdar Ceylaner
Endocrine, Metabolic & Immune Disorders Drug Targets|November 14, 2022
Renal Involvement in H Syndrome, A Rare Cause of Diabetes Mellitus: Case ReportRecep Polat, Ala Ustyol, Rabia Altunbaş, et al.
Turkish Journal of Haematology : Official Journal of Turkish Society of Haematology|July 31, 2023
Hb Andrew-Minneapolis Variant in a Turkish FamilyHamza Sümter, Soycan Mızrak, Serdar Ceylaner, et al.
The Turkish Journal of Pediatrics|July 24, 2018
Microcephaly and developmental delay caused by short-chain acyl-CoA dehydrogenase deficiencyMustafa Kılıç, Saliha Şenel, Kadri Karaer, et al.
Acta Orthopaedica Et Traumatologica Turcica|December 9, 2008
[Autosomal dominant inheritance of congenital dislocation of the hip in 16 members of a family]Gülay Ceylaner, Serdar Ceylaner, Fulya Ustünkan, et al.
International Journal of Gynaecology and Obstetrics: the Official Organ of the International Federation of Gynaecology and Obstetrics|May 18, 2010
Genetic abnormalities in Turkish women with premature ovarian failureGulay Ceylaner, Sunduz Ozlem Altinkaya, Leyla Mollamahmutoglu, et al.
Journal of Clinical Research in Pediatric Endocrinology|August 12, 2021
Compound Heterozygous Variants in <i>FAM111A</i> Cause Autosomal Recessive Kenny-Caffey Syndrome Type 2Erdal Eren, Havva Tezcan Ünlü, Serdar Ceylaner, et al.
Case Reports in Immunology|July 14, 2022
A Case of Common Variable Immunodeficiency with CREBP Gene Mutation without Rubinstein Taybi Syndrome FeaturesUgur Musabak, Serdar Ceylaner, Tuba Erdogan, et al.
Molecular Reproduction and Development|August 31, 2002
Evaluation of segregation patterns of 21;21 Robertsonian translocation along with sex chromosomes and interchromosomal effects in sperm nuclei of carrier by FISH techniqueHasan Acar, M Selman Yildirim, Tülin Cora, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|August 10, 2011
A new variant of a known mutation in two siblings with permanent neonatal diabetes mellitusZehra Aycan, Semra Cetinkaya, Serife Suna Oğuz, et al.
Pageof 25