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Murat Erdogan

Showing results (31-40 of 41) with videos related to

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Molecular Biology Reports|May 20, 2018
Increased vitamin D receptor gene expression and rs11568820 and rs4516035 promoter polymorphisms in autistic disorderBurhan Balta, Hakan Gumus, Ruslan Bayramov, et al.
Medicine|February 17, 2025
Consecutive 5-year outcomes of chorionic villus sampling at a tertiary centerMelda Kuyucu, Kadri Murat Erdogan, Duygu Adiyaman, et al.
European Journal of Medical Genetics|June 9, 2024
Congenital Adrenal Hyperplasia with Combined 21-hydroxylase deficiency and 17α-hydroxylase/17,20-lyase deficiency: An undervirilized maleLeyla Kara, Dilek Cicek, Ulku Gul Siraz, et al.
Indian Journal of Pathology & Microbiology|August 12, 2016
A novel PTCH1 gene mutation in a pediatric patient associated multiple keratocystic odontogenic tumors of the jaws and Gorlin-Goltz syndromeGozde Ozcan, Burhan Balta, Ahmet Ercan Sekerci, et al.
Journal of Obstetrics and Gynaecology : the Journal of the Institute of Obstetrics and Gynaecology|November 27, 2019
Could high levels of cell-free DNA in maternal blood be associated with maternal health and perinatal outcomes?Bahar Konuralp Atakul, Altug Koc, Duygu Adiyaman, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 14, 2021
Evaluation of clinical findings and neurofibromatosis type 1 bright objects on brain magnetic resonance images of 60 Turkish patients with NF1 gene variantsFiliz Hazan, Semra Gürsoy, Aycan Unalp, et al.
Apoptosis : an International Journal on Programmed Cell Death|January 23, 2026
Enhancing the efficacy of VEGF inhibitors by co-inhibition of HIF in the treatment of glioblastomaEmirhan Harbi, Yasemin Yozgat Byrne, Hamza Ugur Bozbey, et al.
Neurogenetics|May 31, 2025
A case series of joubert syndrome evaluated with whole exome sequencing and the utility of optical genome mapping in the diagnosisAslihan Kiraz, Murat Erdogan, Burhan Balta, et al.
European Journal of Ophthalmology|June 2, 2021
Genotype-phenotype correlations in ocular manifestations of Marinesco-Sjögren syndrome: Case report and literature reviewNurettin Bayram, Ayşe Kaçar Bayram, Hülya-Sevcan Daimagüler, et al.
Journal of Medical Virology|July 11, 2022
Analysis of ACE2 and TMPRSS2 coding variants as a risk factor for SARS-CoV-2 from 946 whole-exome sequencing data in the Turkish populationNilgun Duman, Gulten Tuncel, Atil Bisgin, et al.
Pageof 5

Showing results (31-40 of 41) with videos related to

Sort By:
Pageof 5
Molecular Biology Reports|May 20, 2018
Increased vitamin D receptor gene expression and rs11568820 and rs4516035 promoter polymorphisms in autistic disorderBurhan Balta, Hakan Gumus, Ruslan Bayramov, et al.
Medicine|February 17, 2025
Consecutive 5-year outcomes of chorionic villus sampling at a tertiary centerMelda Kuyucu, Kadri Murat Erdogan, Duygu Adiyaman, et al.
European Journal of Medical Genetics|June 9, 2024
Congenital Adrenal Hyperplasia with Combined 21-hydroxylase deficiency and 17α-hydroxylase/17,20-lyase deficiency: An undervirilized maleLeyla Kara, Dilek Cicek, Ulku Gul Siraz, et al.
Indian Journal of Pathology & Microbiology|August 12, 2016
A novel PTCH1 gene mutation in a pediatric patient associated multiple keratocystic odontogenic tumors of the jaws and Gorlin-Goltz syndromeGozde Ozcan, Burhan Balta, Ahmet Ercan Sekerci, et al.
Journal of Obstetrics and Gynaecology : the Journal of the Institute of Obstetrics and Gynaecology|November 27, 2019
Could high levels of cell-free DNA in maternal blood be associated with maternal health and perinatal outcomes?Bahar Konuralp Atakul, Altug Koc, Duygu Adiyaman, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 14, 2021
Evaluation of clinical findings and neurofibromatosis type 1 bright objects on brain magnetic resonance images of 60 Turkish patients with NF1 gene variantsFiliz Hazan, Semra Gürsoy, Aycan Unalp, et al.
Apoptosis : an International Journal on Programmed Cell Death|January 23, 2026
Enhancing the efficacy of VEGF inhibitors by co-inhibition of HIF in the treatment of glioblastomaEmirhan Harbi, Yasemin Yozgat Byrne, Hamza Ugur Bozbey, et al.
Neurogenetics|May 31, 2025
A case series of joubert syndrome evaluated with whole exome sequencing and the utility of optical genome mapping in the diagnosisAslihan Kiraz, Murat Erdogan, Burhan Balta, et al.
European Journal of Ophthalmology|June 2, 2021
Genotype-phenotype correlations in ocular manifestations of Marinesco-Sjögren syndrome: Case report and literature reviewNurettin Bayram, Ayşe Kaçar Bayram, Hülya-Sevcan Daimagüler, et al.
Journal of Medical Virology|July 11, 2022
Analysis of ACE2 and TMPRSS2 coding variants as a risk factor for SARS-CoV-2 from 946 whole-exome sequencing data in the Turkish populationNilgun Duman, Gulten Tuncel, Atil Bisgin, et al.
Pageof 5