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Impact of Fluorescent In Situ Hybridization Aberrations and CLLU1 Expression on the Prognosis of Chronic Lymphocytic Leukemia: Presentation of 156 Patients from Turkey
Turkish journal of haematology, 2018-03, Vol.35 (1), p.61-65
2018
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The Interrelationship Between FYN and miR-128/193a-5p/494 in Imatinib Resistance in Prostate Cancer
Anti-cancer agents in medicinal chemistry, 2023-01, Vol.23 (3), p.360
2023
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Genetic burden and outcome of cystic hygromas detected antenatally: Results of 93 pregnancies from a single center in the Northern Region of Turkey
Journal of medical ultrasound, 2019-10, Vol.27 (4), p.181-186
2019
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Genetic testing can change diagnosis and treatment in children with congenital hypothyroidism
European thyroid journal, 2023-06, Vol.12 (3), p.1-11
2023
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Clinical, cytogenomic, and molecular characterization of isodicentric Y-chromosome and prediction of testicular sperm retrieval outcomes in azoospermic and severe oligozoospermic infertile men
Journal of assisted reproduction and genetics, 2022-12, Vol.39 (12), p.2799-2810
2022
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Correction to: Clinical, cytogenomic, and molecular characterization of isodicentric Y‑chromosome and prediction of testicular sperm retrieval outcomes in azoospermic and severe oligozoospermic infertile men
Journal of assisted reproduction and genetics, 2022-11, Vol.39 (11), p.2685-2685
2022
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Endocrine, sexual and reproductive functions in patients with Klinefelter syndrome compared to non‐obstructive azoospermic patients
International journal of clinical practice (Esher), 2021-08, Vol.75 (8), p.e14294-n/a
2021
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Semiquantitative promoter methylation of MLH1 and MSH2 genes and their impact on sperm DNA fragmentation and chromatin condensation in infertile men
Andrologia, 2021-02, Vol.53 (1), p.e13827-n/a
2021
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Tr-KIT/c-KIT ratio in renal cell carcinoma
Molecular biology reports, 2019-10, Vol.46 (5), p.5287-5294
2019
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Which Ischemic Stroke Subtype Is Associated with Hyperhomocysteinemia?
Journal of stroke and cerebrovascular diseases, 2018-07, Vol.27 (7), p.1921-1929
2018
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Multiscale analysis of SRY‐positive 46,XX testicular disorder of sex development: Presentation of nine cases
Andrologia, 2020-12, Vol.52 (11), p.e13739-n/a
2020
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Chromosomal and Y‐chromosome microdeletion analysis in 1,300 infertile males and the fertility outcome of patients with AZFc microdeletions
Andrologia, 2019-12, Vol.51 (11), p.e13402-n/a
2019
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Could familial Mediterranean fever gene mutations be related to PFAPA syndrome?
Pediatric allergy and immunology, 2016-02, Vol.27 (1), p.78-82
2016
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Vesicourethral reflux-induced renal failure in a patient with ICF syndrome due to a novel DNMT3B mutation
American journal of medical genetics. Part A, 2016-12, Vol.170A (12), p.3253-3257
2016
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Williams Syndrome Associated with Isolated Growth Hormone Deficiency: Is It Just a Coincidence?
Journal of clinical research in pediatric endocrinology, 2017-06, Vol.9 (2), p.18
2017
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A Male Case of Aromatase Deficiency with a Novel CYP19A1 Mutation
Journal of clinical research in pediatric endocrinology, 2017-06, Vol.9 (2), p.2
2017
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A Male Case of Aromatase Deficiency with a Novel CYP19A1 Mutation
Journal of clinical research in pediatric endocrinology, 2017-06, Vol.9 (1), p.2
2017
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Williams Syndrome Associated with Isolated Growth Hormone Deficiency: Is It Just a Coincidence?
Journal of clinical research in pediatric endocrinology, 2017-06, Vol.9 (1), p.18
2017
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Evaluation of the promoter methylation status of hypoxia factor 3A and interleukin-6 genes and expression levels of mir-130b and mir-146b in childhood obesity
Revista da Associação Médica Brasileira, 2022-09, Vol.68 (9), p.1276-1281
2022
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