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Methods in Molecular Biology (Clifton, N.J.)|January 2, 2025
A Comprehensive Bioinformatics Approach to Analysis of Variants: Variant Calling, Annotation, and PrioritizationMerve Nur Koroglu, Kaya BilguvarAmerican Journal of Medical Genetics. Part A|April 10, 2021
Resolution of sclerotic lesions of dysosteosclerosis due to biallelic SLC29A3 variant in a Turkish girlDilek Uludağ Alkaya, Evren Akpınar, Kaya Bilguvar, et al.Pediatric Radiology|September 27, 2014
Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type: longitudinal observation of radiographic findings in a child heterozygous for a KIF22 mutationBeyhan Tüysüz, Saliha Yılmaz, Tuğba Erener-Ercan, et al.Neurosurgery|February 10, 2007
Genetics of intracranial aneurysmsBrian V Nahed, Mohamad Bydon, Ali K Ozturk, et al.American Journal of Medical Genetics. Part A|May 2, 2013
Spondyloepimetaphyseal dysplasia Pakistani type: expansion of the phenotypeBeyhan Tüysüz, Saliha Yılmaz, Ece Gül, et al.Omics : a Journal of Integrative Biology|September 5, 2023
Toward Precision Oncology in Glioblastoma with a Personalized Cancer Genome Reporting Tool and Genetic Changes Identified by Whole Exome SequencingOnur Erdogan, Şeyma Çolakoğlu Özkaya, Can Erzik, et al.Turkish Archives of Pediatrics|August 11, 2022
Severe Phenotype in Patients with X-linked Hydrocephalus Caused by a Missense Mutation in L1CAMBeyhan Tüysüz, Adife Gülhan Ercan-Sençicek, Emre Özer, et al.Rheumatology International|May 13, 2014
Primary hypertrophic osteoarthropathy caused by homozygous deletion in HPGD gene in a family: changing clinical and radiological findings with long-term follow-upBeyhan Tüysüz, Saliha Yılmaz, Özgür Kasapçopur, et al.Journal of Neurosurgery|September 10, 2016
Familial occurrence of brain arteriovenous malformation: a novel ACVRL1 mutation detected by whole exome sequencingBaran Yılmaz, Zafer Orkun Toktaş, Akın Akakın, et al.Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|April 2, 2008
Therapeutic efficacy of Ac-DMQD-CHO, a caspase 3 inhibitor, for rat spinal cord injuryOsman Akdemir, Ismail Berksoy, Alper Karaoğlan, et al.Pageof 13