15 Artykułów
Review article
Original article
Otwarty dostęp | 23 mar 2021
The utility of whole exome sequencing in diagnosing pediatric neurological disorders
Otwarty dostęp | 23 mar 2021
Array-comparative genomic hybridization results in clinically affected cases with apparently balanced chromosomal rearrangements
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Otwarty dostęp | 23 mar 2021
Do we use methylation of NFATC1 and FOS genes as a biomarker for postmenopausal osteoporosis?
oraz
Otwarty dostęp | 23 mar 2021
Influence of potential gene polymorphisms on propofol dosage regimen in patients undergoing abdominal hysterectomy
, , , , oraz
Otwarty dostęp | 23 mar 2021
Investigation of the relationship of TNFRSF11A gene polymorphisms with breast cancer development and metastasis risk in patients with BRCA1 or BRCA2 pathogenic variants living in the Trakya region of Turkey
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Otwarty dostęp | 23 mar 2021
Pros and cons for fluorescent in situ hybridization, karyotyping and next generation sequencing for diagnosis and follow-up of multiple myeloma
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Otwarty dostęp | 23 mar 2021
Evaluation of methylation profiles of an epidermal growth factor receptor gene in a head and neck squamous cell carcinoma patient group
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Case report
Otwarty dostęp | 23 mar 2021
Fetal cystic hygroma associated with terminal 2p25.1 duplication and terminal 3p25.3 deletion: Cytogenetic, fluorescent in situ hybridization and microarray familial characterization of two different chromosomal structural rearrangements
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Otwarty dostęp | 23 mar 2021
Familial non-autoimmune hyperthyroidism in family members across four generations due to a novel disease-causing variant in the thyrotropin receptor gene
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Otwarty dostęp | 23 mar 2021
Bilateral renal angiomyolipomas and subependymal giant cell astrocytoma associated with tuberous sclerosis complex: A case report and review of the literature
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Otwarty dostęp | 23 mar 2021
Two novel CEBPA mutations in a Turkish patient with acute myeloid leukemia
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Otwarty dostęp | 23 mar 2021
Case report of a successful pregnancy in a cystic fibrosis patient with the c.1521_1523delCTT/c.3718-2477C>t genotypes
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Otwarty dostęp | 23 mar 2021
Osteopetrorickets in an infant with coexistent congenital cytomegalovirus infection
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