TWO CASES OF ALLELES WITH COMPLEX GENOTYPES AMONG CYSTIC FIBROSIS PATIENTS FROM CROATIA
Tanacković G1, Barišić I2, Knežević J1, Pavelić J1,*
*Corresponding Author: Professor Dr. Jasminka Pavelić, Division of Molecular Medicine, Rudjer Bošković Institute, Bijenička cesta 54, HR-10002 Zagreb, Croatia; Tel: +385-1-4560-926; Fax: +385-1-456-1010; E-mail: jpavelic@rudjer.irb.hr
page: 3

MATERIALS AND METHODS

Blood samples were obtained from the Department of Pediatrics at the Children’s Hospital, Zagreb, Croatia. The diagnoses were based on clinical presentation and positive sweat Cl test (over 60 mmol/L). Genomic DNA was isolated by a standard salting out procedure [5]. The mutations were detected by heteroduplex analysis and restriction fragment length polymorphism (RFLP) [6,7]. The polymorphisms were detected by denaturing gradient gel electrophoresis (DGGE) [8].




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