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International Journal of Molecular Sciences
|
January 28, 2026
Biallelic Truncating <i>DNAH14</i> Variant in Siblings with Neurodevelopmental Disorder and Predominant Ataxia: Clinical Report and Literature Review
Savas Baris, Mustafa Dogan, Kerem Terali, et al.
The Tohoku Journal of Experimental Medicine
|
December 2, 2004
Plasma leptin levels in rats with pancreatitis
Nihat Yavuz, Ethem Unal, Kemal Memisoglu, et al.
Molecular Syndromology
|
February 15, 2024
A Deeper Insight into <i>COL4A3</i>, <i>COL4A4</i>, and <i>COL4A5</i> Variants and Genotype-Phenotype Correlation of a Turkish Cohort with Alport Syndrome
Cuneyd Yavas, Nehir Ozdemir Ozgenturk, Mustafa Dogan, et al.
Clinical Nephrology
|
April 23, 2026
Evaluation of epicardial adipose tissue in children with chronic kidney disease
Mehmet Baha Aytac, Mustafa Dogan, Sule Ayas Ergul, et al.
Brain & Development
|
July 9, 2025
Biallelic novel CCDC186 loss-of-function variant disrupting the gene function causes neurodevelopmental phenotype and review of the literature
Alper Gezdirici, Sultan Buse Turk, Tuna Eren Esen, et al.
Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology
|
June 7, 2014
Evaluation of ovarian reserve in Hashimoto's thyroiditis
Abdullah Tuten, Esra Hatipoglu, Mahmut Oncul, et al.
Molecular Syndromology
|
January 7, 2026
Molecular and Clinical Profiles of Patients with RASopathies: Targeted Next-Generation Sequencing Panel Results and Identification of 14 Novel Disease-Causing Variants
Kubra Ates, Murat Ozturk, Zeynep Esener, et al.
Forensic Science International. Genetics
|
May 21, 2021
Genetic relationships of Southwest Asian and Mediterranean populations
Kenneth K Kidd, Ozlem Bulbul, Cemal Gurkan, et al.
Life (Basel, Switzerland)
|
March 28, 2026
Phenotype-Driven Next-Generation Sequencing and Structure-Based In Silico Analysis Reveal Disease-Specific Diagnostic Yield and Genotype-Phenotype Correlations in Inherited Kidney Diseases
Savas Baris, Kerem Terali, Serdar Bozlak, et al.
SAGE Open Medicine
|
April 25, 2022
A 5-year surveillance of healthcare-associated infections in a university hospital: A retrospective analysis
Ilknur Erdem, Ilker Yıldırım, Birol Safak, et al.
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Search research articles
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Showing results (71-80 of 96) with videos related to
Sort By:
Page
of 10
International Journal of Molecular Sciences
|
January 28, 2026
Biallelic Truncating <i>DNAH14</i> Variant in Siblings with Neurodevelopmental Disorder and Predominant Ataxia: Clinical Report and Literature Review
Savas Baris, Mustafa Dogan, Kerem Terali, et al.
The Tohoku Journal of Experimental Medicine
|
December 2, 2004
Plasma leptin levels in rats with pancreatitis
Nihat Yavuz, Ethem Unal, Kemal Memisoglu, et al.
Molecular Syndromology
|
February 15, 2024
A Deeper Insight into <i>COL4A3</i>, <i>COL4A4</i>, and <i>COL4A5</i> Variants and Genotype-Phenotype Correlation of a Turkish Cohort with Alport Syndrome
Cuneyd Yavas, Nehir Ozdemir Ozgenturk, Mustafa Dogan, et al.
Clinical Nephrology
|
April 23, 2026
Evaluation of epicardial adipose tissue in children with chronic kidney disease
Mehmet Baha Aytac, Mustafa Dogan, Sule Ayas Ergul, et al.
Brain & Development
|
July 9, 2025
Biallelic novel CCDC186 loss-of-function variant disrupting the gene function causes neurodevelopmental phenotype and review of the literature
Alper Gezdirici, Sultan Buse Turk, Tuna Eren Esen, et al.
Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology
|
June 7, 2014
Evaluation of ovarian reserve in Hashimoto's thyroiditis
Abdullah Tuten, Esra Hatipoglu, Mahmut Oncul, et al.
Molecular Syndromology
|
January 7, 2026
Molecular and Clinical Profiles of Patients with RASopathies: Targeted Next-Generation Sequencing Panel Results and Identification of 14 Novel Disease-Causing Variants
Kubra Ates, Murat Ozturk, Zeynep Esener, et al.
Forensic Science International. Genetics
|
May 21, 2021
Genetic relationships of Southwest Asian and Mediterranean populations
Kenneth K Kidd, Ozlem Bulbul, Cemal Gurkan, et al.
Life (Basel, Switzerland)
|
March 28, 2026
Phenotype-Driven Next-Generation Sequencing and Structure-Based In Silico Analysis Reveal Disease-Specific Diagnostic Yield and Genotype-Phenotype Correlations in Inherited Kidney Diseases
Savas Baris, Kerem Terali, Serdar Bozlak, et al.
SAGE Open Medicine
|
April 25, 2022
A 5-year surveillance of healthcare-associated infections in a university hospital: A retrospective analysis
Ilknur Erdem, Ilker Yıldırım, Birol Safak, et al.
Page
of 10