المؤلفون: N. Paylar, Osman Demirhan, Erdal Tunç, Ismail Yildiz, Ali İrfan Güzel, Yahya Sağliker

المساهمون: RTEÜ, Tıp Fakültesi, Temel Tıp Bilimleri Bölümü, Güzel, Ali İrfan, Çukurova Üniversitesi

المصدر: Volume: 47, Issue: 1 13-21
Turkish Journal of Medical Sciences

مصطلحات موضوعية: 0301 basic medicine, Male, medicine.medical_specialty, Turkey, Sequence analysis, 030232 urology & nephrology, Bioinformatics, 03 medical and health sciences, Exon, 0302 clinical medicine, Chronic kidney disease, Sagliker syndrome,CaSR gene,chromosomal abnormalities,chronic kidney disease,nucleotide alterations, Genetic predisposition, Medicine, Humans, Genetic Predisposition to Disease, Renal Insufficiency, Chronic, Cerrahi, Calcium metabolism, Chromosome Aberrations, business.industry, Chromosomal abnormalities, Cytogenetics, Chromosome, General Medicine, Exons, Syndrome, Nucleotide alterations, medicine.disease, 030104 developmental biology, Case-Control Studies, Cytogenetic Analysis, Cancer research, Secondary hyperparathyroidism, Female, Hyperparathyroidism, Secondary, Sagliker syndrome, CaSR gene, business, Receptors, Calcium-Sensing, Kidney disease

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cae2e934d3d1ff72c2dd593eadfc2248
https://hdl.handle.net/11436/4923