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European Journal of Medical Genetics|May 12, 2016
Spectrum of clinical manifestations in two young Turkish patients with congenital generalized lipodystrophy type 4Gulcin Akinci, Haluk Topaloglu, Baris Akinci, et al.
Molecular Biology Reports|December 29, 2023
Association between vitamin D receptor gene FokI polymorphism and mortality in patients with sepsisSukriye Miray Kilincer Bozgul, Durdugul Ayyildiz Emecen, Funda Karbek Akarca, et al.
Clinical Rheumatology|January 9, 2019
Correction to: Evaluation of the effects of miRNAs in familial Mediterranean feverHacer Orsdemir Hortu, Emin Karaca, Betul Sozeri, et al.
Clinical Rheumatology|February 15, 2018
Evaluation of the effects of miRNAs in familial Mediterranean feverHacer Orsdemir Hortu, Emin Karaca, Betul Sozeri, et al.
American Journal of Medical Genetics. Part A|December 1, 2020
A rare cause of syndromic short stature: 3M syndrome in three familiesEsra Isik, Duygu Arican, Tahir Atik, et al.
Archives of Dermatological Research|March 2, 2025
Molecular insights into genodermatoses: Genetic findings from 43 patientsArzu Deniz Sama, Enise Avci Durmusalioglu, Esra Isik, et al.
BMC Pharmacology & Toxicology|June 5, 2026
Intravenous diazepam application in a departmental convulsive status epilepticus protocol with CYP2C19 polymorphisms: a pediatric prospective cohort studyMuazzez Seker Gezici, Caner Turan, Durdugul Ayyildiz Emecen, et al.
Clinical Genetics|October 22, 2024
Utility of Optical Genome Mapping in Repeat DisordersMehmet Burak Mutlu, Taner Karakaya, Hamide Betül Gerik Çelebi, et al.
Journal of Clinical Research in Pediatric Endocrinology|June 3, 2024
Molecular Genetic Diagnosis with Targeted Next Generation Sequencing in a Cohort of Turkish Osteogenesis Imperfecta Patients and their Genotype-phenotype CorrelationSamim Özen, Damla Gökşen, Ferda Evin, et al.
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