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MTA Fillapex’in İn Vitro Genotoksisitesinin Değerlendirilmesinin Sistematik İncelemesi.
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- Turkiye Klinikleri Journal of Dental Sciences, 2022, v. 28, n. 2, p. 372, doi. 10.5336/dentalsci.2021-83767
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- Article
The frequencies of Y chromosome microdeletions in infertile males.
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- Turkish Journal of Urology, 2018, v. 44, n. 5, p. 389, doi. 10.5152/tud.2018.73669
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- Article
Neonatal Diabetes, Congenital Hypothyroidism, and Congenital Glaucoma Coexistence: A Case of GLIS3 Mutation.
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- Journal of Clinical Research in Pediatric Endocrinology, 2023, v. 15, n. 4, p. 426, doi. 10.4274/jcrpe.galenos.2022.2021-12-19
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- Article
Parental Karyotype and Genetic Markers for Thrombophilia in Recurrent Miscarriage.
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- Journal of the Turkish-German Gynecological Association, 2008, v. 9, n. 3, p. 139
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- Article
Current Advances in Breast Cancer: Implications for Developing New Treatment Strategies Through Epi-Drugs on the Road to Modifying the Epigenome.
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- Journal of Clinical Practice & Research, 2023, v. 45, n. 5, p. 427, doi. 10.14744/cpr.2023.08208
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- Article
A Rare Cause of Hypotonia: 49,XXXXX (Pentasomy X).
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- Journal of Pediatric Academy (J. Pediatr. Acad.), 2023, v. 4, n. 4, p. 149, doi. 10.4274/jpea.2023.230
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- Article
Investigation of CDKL5 Gene Mutations in Autistic Patients Accompanied with Intractable Seizures, Autistic Disorder and Seizure in Infancy and Early Childhood.
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- Cumhuriyet Medical Journal, 2022, v. 44, n. 2, p. 165, doi. 10.7197/cmj.1121531
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- Article
A New Translocation in a Case of Recurrent Pregnancy Loss: t(2;7)(q31;p21).
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- Gazi Medical Journal, 2024, v. 35, p. 67
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- Article
A Case of Cardiophaciocutaneous Syndrome without Cardiac Manifestations.
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- Gazi Medical Journal, 2024, v. 35, p. 79
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- Article
The Case with the Novel NALCN Variant.
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- Gazi Medical Journal, 2024, v. 35, p. 79
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- Article
Case Report: Patient with Merosin-Deficient Congenital Muscular Dystrophy with Occipital Lissencephaly.
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- Gazi Medical Journal, 2024, v. 35, p. 77
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- Article
Duplication of 1q21.3q25.3 in a Newborn with Multiple Congenital Anomalies.
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- Gazi Medical Journal, 2024, v. 35, p. 78
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- Article
Hereditary Hyperekplexia: Three Patients from Kayseri, Middle Anatolia and Three Different Genetic Findings by Different Methodology.
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- Gazi Medical Journal, 2024, v. 35, p. 77
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- Article
A Case of Char Syndrome with a Novel TFAP2B Variant.
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- Gazi Medical Journal, 2024, v. 35, p. 55
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- Article
Diagnosis of Townes-Brocks Syndrome in a Turkish Adolescent with End-Stage Renal Failure.
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- Gazi Medical Journal, 2024, v. 35, p. 52
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- Article
Blended Phenotype in a Case with Brain Malformation, Neurodevelopmental Disorder and Epilepsy.
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- Gazi Medical Journal, 2024, v. 35, p. 49
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- Article
A Novel Homozygous Variant in TBC1D24 Gene: A Case Report.
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- Gazi Medical Journal, 2024, v. 35, p. 53
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- Article
An Interesting Family: A Patient with Blended Phenotype with Sexual Development Disorder and Coenzyme Q10 Deficiency and His Sibling Diagnosed with Joubert.
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- Gazi Medical Journal, 2024, v. 35, p. 51
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- Article
Detection of Somatic Variant in PIK3R2 Gene in a Patient Followed with Galactosemia.
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- Gazi Medical Journal, 2024, v. 35, p. 52
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- Article
A Rare Variant in the CDH2 Gene: The Second ACOGS Case from Türkiye.
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- Gazi Medical Journal, 2024, v. 35, p. 51
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- Article
Adaptor Protein Complex 4-associated Hereditary Spastic Paraplegia: A Case Series of Seven Patients.
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- Gazi Medical Journal, 2024, v. 35, p. 46
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- Article
Meeting Reports: Notes and commentaries on Turkish Medical Genetics Association and Cyprus Turkish Genetic Union Meeting.
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- Gazi Medical Journal, 2020, v. 31, n. 3, p. 1
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- Article
Evaluation of aortic intima-media thickness in newborns with Down syndrome.
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- Advances in Clinical & Experimental Medicine, 2017, v. 26, n. 8, p. 1253, doi. 10.17219/acem/68677
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- Article
Mesenchymal stem cells from adipose tissue prone to lose their stemness associated markers in obesity related stress conditions.
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- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-70127-w
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- Article
The Association of Brain-Derived Neurotrophic Factor Gene Polymorphism with Obstructive Sleep Apnea Syndrome and Obesity.
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- Lung, 2016, v. 194, n. 5, p. 839, doi. 10.1007/s00408-016-9894-z
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- Article
Recurrent symptomatic urolithiasis in a patient with cystic fibrosis.
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- Pediatric Nephrology, 2024, v. 39, n. 12, p. 3467, doi. 10.1007/s00467-024-06433-2
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- Article
A rare cause of membranoproliferative patterns of injury in siblings with steroid-resistant nephrotic syndrome: Answers.
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- Pediatric Nephrology, 2021, v. 36, n. 12, p. 4029, doi. 10.1007/s00467-021-05154-0
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- Article
A rare cause of membranoproliferative patterns of injury in siblings with steroid-resistant nephrotic syndrome: Questions.
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- 2021
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- Case Study
Prenatal VSD Tanısı Alan Olguların Sonuçlarının Değerlendirilmesi.
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- Erciyes Medical Journal / Erciyes Tip Dergisi, 2012, v. 34, n. 3, p. 111, doi. 10.5152/etd.2012.34
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- Article
Amniyotik Bant Sekanslı Olguya Genetik Yaklaşım.
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- Erciyes Medical Journal / Erciyes Tip Dergisi, 2010, v. 32, n. 1, p. 61
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- Article
A very rare cause of arthrogryposis multiplex congenita: a novel mutation in TOR1A.
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- Journal of Pediatric Endocrinology & Metabolism, 2022, v. 35, n. 6, p. 845, doi. 10.1515/jpem-2021-0766
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- Article
A retrospective study on the clinical and molecular outcomes of calpainopathy in a Turkish patient cohort.
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- Turkish Journal of Medical Sciences, 2024, v. 54, n. 1, p. 86, doi. 10.55730/1300-0144.5769
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- Article
Sendromik olmayan ailesel işitme kaybının genetik temelinin araştırılması.
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- Türk Pediatri Arşivi, 2017, v. 52, n. 3, p. 122, doi. 10.5152/TurkPediatriArs.2017.4254
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- Article
Current and Future Therapeutic Strategies for Limb Girdle Muscular Dystrophy Type R1: Clinical and Experimental Approaches.
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- Pathophysiology, 2021, v. 28, n. 2, p. 238, doi. 10.3390/pathophysiology28020016
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- Article
Investigation of Relation Between MDR1 Gene and Ankylosing Spondylitis: Case Control Research.
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- Turkiye Klinikleri Journal of Medical Sciences, 2022, v. 42, n. 3, p. 213, doi. 10.5336/medsci.2021-87249
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- Article
ANADOLU'DAKİ TIBBIN DOĞUŞU, DÜNYADAKİ İLK TIP OKULU OLARAK GEVHER NESİBE TIP MEDRESESİ VE DARÜŞŞİFASI.
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- Bilimname, 2019, v. 39, n. 3, p. 79, doi. 10.28949/bilimname.594087
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- Article
The effect of cytokine leukemia-inhibitory factor (LIF) and interleukin-11 (IL-11) gene expression on the primary infertility related to polycystic ovary syndrome, Tubal factor, and Unexplained infertility in Turkish women.
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- Egyptian Journal of Medical Human Genetics, 2021, v. 22, n. 1, p. 1, doi. 10.1186/s43042-021-00201-9
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- Article
Loss of dermatan-4-sulfotransferase 1 (D4ST1/ CHST14) function represents the first dermatan sulfate biosynthesis defect, 'dermatan sulfate-deficient adducted thumb-clubfoot syndrome'.
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- Human Mutation, 2011, v. 32, n. 4, p. 484, doi. 10.1002/humu.21440
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- Article
Reclassification of Hereditary Cancer Genes Variants.
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- Turkish Journal of Oncology / Türk Onkoloji Dergisi, 2022, v. 37, n. 4, p. 462, doi. 10.5505/tjo.2022.3529
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- Article