Found: 19
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Evaluation of CNTNAP2 gene rs2107856 polymorphism in Turkish population with pseudoexfoliation syndrome.
- Published in:
- International Ophthalmology, 2019, v. 39, n. 1, p. 167, doi. 10.1007/s10792-017-0800-3
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- Publication type:
- Article
The Role of Molecular Karyotyping in the Genetic Etiology of Autism.
- Published in:
- Turk Psikiyatri Dergisi, 2017, v. 28, n. 3, p. 1, doi. 10.5080/u18239
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- Publication type:
- Article
Effect of CTLA-4 and TNF-α Gene Polymorphisms on Inhibitor Development in a Turkish Cohort of Severe Hemophilia A Cases with Intron 22 Inversion Mutation: An Analytical Study.
- Published in:
- Turkiye Klinikleri Journal of Medical Sciences, 2022, v. 42, n. 3, p. 159, doi. 10.5336/medsci.2021-86664
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- Publication type:
- Article
Hemofili B Moleküler Analizinde Türkiye Deneyimi: F9 Gen Mutasyon Spektrumu ve Genotip-Fenotip İlişkisi.
- Published in:
- Turkiye Klinikleri Journal of Medical Sciences, 2020, v. 40, n. 3, p. 334, doi. 10.5336/medsci.2020-75066
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- Publication type:
- Article
Factor 8 Gene Mutation Spectrum of 270 Patients with Hemophilia A: Identification of 36 Novel Mutations.
- Published in:
- Turkish Journal of Hematology, 2020, v. 37, n. 3, p. 145, doi. 10.4274/tjh.galenos.2020.2019.0262
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- Publication type:
- Article
Clinical and molecular findings in children and young adults with persistent low alkaline phosphatase concentrations.
- Published in:
- Annals of Clinical Biochemistry, 2021, v. 58, n. 4, p. 335, doi. 10.1177/00045632211000102
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- Publication type:
- Article
Evaluation of Differences of Fast and High Accuracy Base Calling Models of Guppy on Variant Calling Using Low Coverage WGS Data.
- Published in:
- International Journal of Life Sciences & Biotechnology (2651-4621), 2023, v. 6, n. 3, p. 276, doi. 10.38001/ijlsb.1308355
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- Publication type:
- Article
Atipik Teratoid Rabdoid Tümörlü Olgularda Demografik, Klinik, Patolojik Özelliklerin ve HSNF5 (SMARCB1)/INI1 Gen Mutasyonlarının Araştırılması.
- Published in:
- Turkiye Klinikleri Journal of Pediatrics / Türkiye Klinikleri Pediatri Dergisi, 2020, v. 29, n. 3, p. 139, doi. 10.5336/pediatr.2019-72772
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- Publication type:
- Article
Immunodeficiency in a Child with Alström Syndrome.
- Published in:
- 2018
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- Publication type:
- case study
A genome‐wide association study in Puerto Ricans suggests new risk loci for Alzheimer disease.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2023, v. 19, p. 1, doi. 10.1002/alz.080233
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- Publication type:
- Article
A new risk locus on chromosome 1 is suggested by genome‐wide association study in Peruvians for Alzheimer disease.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2023, v. 19, p. 1, doi. 10.1002/alz.077859
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- Publication type:
- Article
A genome‐wide association study in Puerto Ricans suggests new risk loci for Alzheimer disease.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2023, v. 19, p. 1, doi. 10.1002/alz.080233
- By:
- Publication type:
- Article
A new risk locus on chromosome 1 is suggested by genome‐wide association study in Peruvians for Alzheimer disease.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2023, v. 19, p. 1, doi. 10.1002/alz.077859
- By:
- Publication type:
- Article
African‐ancestry based polygenic risk scores improve Alzheimer disease risk prediction in individuals of African Ancestry.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2022, v. 18, n. 3, p. 1, doi. 10.1002/alz.067457
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- Publication type:
- Article
A Novel Molecular Indicator for Inhibitor Development in Haemophilia A.
- Published in:
- Journal of Pediatric Research, 2021, v. 8, n. 2, p. 102, doi. 10.4274/jpr.galenos.2020.59354
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- Publication type:
- Article
Evaluation of Six Patients with Chromosome 18 Structural Anomalies and Novel Findings.
- Published in:
- Journal of Pediatric Research, 2020, v. 7, n. 4, p. 267, doi. 10.4274/jpr.galenos.2019.38278
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- Publication type:
- Article
Evaluation of Six Patients with Chromosome 18 Structural Anomalies and Novel Findings.
- Published in:
- Journal of Pediatric Research, 2020, v. 7, n. 4, p. 267, doi. 10.4274/jpr.galenos.2019.38278
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- Publication type:
- Article
Genome-wide association analysis and admixture mapping in a Puerto Rican cohort supports an Alzheimer disease risk locus on chromosome 12.
- Published in:
- Frontiers in Aging Neuroscience, 2024, p. 1, doi. 10.3389/fnagi.2024.1459796
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- Publication type:
- Article
The Role of Molecular Karyotyping in the Genetic Etiology of Autism.
- Published in:
- Turkish Journal of Psychiatry, 2017, v. 28, n. 3, p. 1, doi. 10.5080/u18239
- By:
- Publication type:
- Article