Authors:
Bouba, I
Koptides, M
Mean, R
Costi, CE
Demetriou, K
Georgiou, I
Pierides, A
Siamopoulos, K
Deltas, CC
Citation: I. Bouba et al., Novel PKD1 deletions and missense variants in a cohort of Hellenic polycystic kidney disease families, EUR J HUM G, 9(9), 2001, pp. 677-684
Citation: K. Angelopoulou et al., Prevalence of genetic mutations that predispose to thrombophilia in a Greek Cypriot population, CL APPL T-H, 6(2), 2000, pp. 104-107
Authors:
Koptides, M
Mean, R
Demetriou, K
Pierides, A
Deltas, CC
Citation: M. Koptides et al., Genetic evidence for a trans-heterozygous model for cystogenesis in autosomal dominant polycystic kidney disease, HUM MOL GEN, 9(3), 2000, pp. 447-452
Citation: M. Koptides et Cc. Deltas, Autosomal dominant polycystic kidney disease: molecular genetics and molecular pathogenesis, HUM GENET, 107(2), 2000, pp. 115-126
Authors:
Koptides, M
Hadjimichael, C
Koupepidou, P
Pierides, A
Deltas, CC
Citation: M. Koptides et al., Germinal and somatic mutations in the PKD2 gene of renal cysts in autosomal dominant polycystic kidney disease, HUM MOL GEN, 8(3), 1999, pp. 509-513
Authors:
Koptides, M
Constantinides, R
Kyriakides, G
Hadjigavriel, M
Patsalis, PC
Pierides, A
Deltas, CC
Citation: M. Koptides et al., Loss of heterozygosity in polycystic kidney disease with a missense mutation in the repeated region of PKD1, HUM GENET, 103(6), 1998, pp. 709-717