15 Articoli
Review article
Original article
Accesso libero | 23 mar 2021
The utility of whole exome sequencing in diagnosing pediatric neurological disorders
Accesso libero | 23 mar 2021
Array-comparative genomic hybridization results in clinically affected cases with apparently balanced chromosomal rearrangements
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Accesso libero | 23 mar 2021
Do we use methylation of NFATC1 and FOS genes as a biomarker for postmenopausal osteoporosis?
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Accesso libero | 23 mar 2021
Influence of potential gene polymorphisms on propofol dosage regimen in patients undergoing abdominal hysterectomy
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Accesso libero | 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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Accesso libero | 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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Accesso libero | 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
Accesso libero | 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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Accesso libero | 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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Accesso libero | 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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Accesso libero | 23 mar 2021
Two novel CEBPA mutations in a Turkish patient with acute myeloid leukemia
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Accesso libero | 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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Accesso libero | 23 mar 2021
Osteopetrorickets in an infant with coexistent congenital cytomegalovirus infection
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