Found: 12
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Genetics of Hypokinetic Diseases and Genetic Counseling.
- Published in:
- Gazi Medical Journal, 2024, v. 35, p. 2
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- Publication type:
- Article
Rare Case: Nablus Mask-Like Facial Syndrome.
- Published in:
- Gazi Medical Journal, 2024, v. 35, p. 43
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- Publication type:
- Article
PGT-M for Neurogenetic Diseases with Monogenic Inheritance: Applications and Experiences.
- Published in:
- Gazi Medical Journal, 2024, v. 35, p. 49
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- Publication type:
- Article
Evaluation of Genetic Disorders Associated with Epilepsy in Children.
- Published in:
- Gazi Medical Journal, 2024, v. 35, p. 50
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- Publication type:
- Article
A Case of 48,XXYY Syndrome Presenting with ADHD.
- Published in:
- Gazi Medical Journal, 2024, v. 35, p. 50
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- Publication type:
- Article
3q29 microdeletion syndrome associated with developmental delay and pulmonary stenosis: a case report.
- Published in:
- 2022
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- Publication type:
- Case Study
MLPA Method does not Always Confirm the Results of aCGH: A Study of KANSL1 Gene Deletion Patients.
- Published in:
- Gazi Medical Journal, 2022, v. 33, n. 2, p. 163, doi. 10.12996/gmj.2022.37
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- Publication type:
- Article
Ethical Issues Encountered within the Context of an Adrenoleukodystrophy Case.
- Published in:
- Gazi Medical Journal, 2020, v. 31, n. 2, p. 219, doi. 10.12996/gmj.2020.59
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- Publication type:
- Article
Increased nuchal translucency and pregnancy outcomes: experience of Baskent University Ankara Hospital.
- Published in:
- Turkish Journal of Obstetrics & Gynecology, 2019, v. 16, n. 2, p. 100, doi. 10.4274/tjod.galenos.2019.51482
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- Publication type:
- Article
The analysis of the termination of pregnancies at and after ten weeks of gestation - a monocenter study.
- Published in:
- Perinatal Journal / Perinatoloji Dergisi, 2019, v. 27, n. 1, p. 14, doi. 10.2399/prn.19.0271003
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- Publication type:
- Article
Neonatal cerebral sinovenous thrombosis: Two cases, two different gene polymorphisms and risk factors.
- Published in:
- Turkish Journal of Pediatrics, 2017, v. 59, n. 1, p. 71, doi. 10.24953/turkjped.2017.01.012
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- Publication type:
- Article
Effect of Hereditary Hemochromatosis Gene H63D and C282Y Mutations on Iron Overload in Sickle Cell Disease Patients.
- Published in:
- Turkish Journal of Hematology, 2016, v. 33, n. 4, p. 320, doi. 10.4274/tjh.2015.0254
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- Publication type:
- Article