Found: 15
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Y chromosome polymorphism in Turkish patients with reproductive problems: a genetic centre experience.
- Published in:
- European Research Journal, 2023, v. 9, n. 4, p. 725, doi. 10.18621/eurj.1130666
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- Article
Comprehensive Genetic Analysis of RASopathy in the Era of Next-Generation Sequencing and Definition of a Novel Likely Pathogenic KRAS Variation.
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- Molecular Syndromology, 2022, v. 13, n. 2, p. 88, doi. 10.1159/000520722
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- Article
Wiedemann-Steiner Syndrome as a Differential Diagnosis of Cornelia de Lange Syndrome Using Targeted Next-Generation Sequencing: A Case Report.
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- Molecular Syndromology, 2021, v. 12, n. 1, p. 46, doi. 10.1159/000511971
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- Article
The Application of Next Generation Sequencing Maturity Onset Diabetes of the Young Gene Panel in Turkish Patients from Trakya Region.
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- Journal of Clinical Research in Pediatric Endocrinology, 2021, v. 13, n. 3, p. 320, doi. 10.4274/jcrpe.galenos.2021.2020.0285
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- Article
Prenatal Sitogenetik Anormallikler ve Ultrasonografik olarak Saptanan Fetal Anomalilerin Korelasyonu.
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- Osmangazi Journal of Medicine / Osmangazi Tip Dergisi, 2022, v. 44, n. 5, p. 682, doi. 10.20515/otd.1055810
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- Article
Sendromik Olmayan Konjenital Yarık Damak-Dudak Bulunan Hastalarda Kopya Sayısı Varyasyonlarının Belirlenmesi.
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- Osmangazi Journal of Medicine / Osmangazi Tip Dergisi, 2021, v. 43, n. 5, p. 462, doi. 10.20515/otd.910654
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- Article
Investigation of Genes Associated With Atherosclerosis in Patients With Systemic Lupus Erythematosus.
- Published in:
- Archives of Rheumatology, 2021, v. 36, n. 2, p. 287, doi. 10.46497/ArchRheumatol.2021.8024
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- Article
The Correlation of Cystic Fibrosis Screening Test Results with Ultrasonographically Detected Fetal Anomalies in Prenatal Diagnosis.
- Published in:
- Medical Journal of Bakirkoy, 2023, v. 19, n. 2, p. 191, doi. 10.4274/BMJ.galenos.2023.2023.1-10
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- Article
The Correlation of Cystic Fibrosis Screening Test Results with Ultrasonographically Detected Fetal Anomalies in Prenatal Diagnosis.
- Published in:
- Medical Journal of Bakirkoy, 2023, v. 19, n. 2, p. 191, doi. 10.4274/BMJ.galenos.2023.2023.1-10
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- Article
Investigation of the Relationship Between Genome Wide Association Studies-derived Polymorphisms and Differentiated Thyroid Cancer Risk in a Turkish Population.
- Published in:
- Gazi Medical Journal, 2021, v. 32, n. 4, p. 547, doi. 10.12996/gmj.2021.123
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- Article
17q21.31 deletion including partially EFTUD2 gene detected by arrayCGH in a patient with Mandibulofacial dysostosis type Guion-Almeida.
- Published in:
- Gazi Medical Journal, 2019, v. 30, n. 4a, p. P7
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- Article
Boy Kısalığı Ön Tanısı Alan Hastalarda Kopya Sayısı Değişimleri.
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- Gazi Medical Journal, 2019, v. 30, n. 4a, p. P5
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- Article
Investigation of the Genetic Etiology in Idiopathic Generalized Epileptic Disorders by Targeted Next-generation Sequencing Technique.
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- Balkan Medical Journal, 2023, v. 40, n. 1, p. 13, doi. 10.4274/balkanmedj.galenos.2022.2022-7-55
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- Article
Comprehensive Genetic Analysis Results of TSC1/TSC2 Genes in Patients with Clinical Suspicion of Tuberous Sclerosis Complex and Definition of 3 Novel Variants.
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- Balkan Medical Journal, 2021, v. 38, n. 6, p. 341, doi. 10.5152/balkanmedj.2021.21092
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- Article
Two Cases of Cystic Fibrosis with Compound Heterozygous Variants Reported for the First Time.
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- Balkan Medical Journal, 2020, v. 37, n. 5, p. 297, doi. 10.4274/balkanmedj.galenos.2020.2019.11.128
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- Article