Authors: Bekir, NA Gungor, K Guran, S

Citation: Na. Bekir et al., A DIDMOAD syndrome family with juvenile glaucoma and myopia findings, ACT OPHTH S, 78(4), 2000, pp. 480-482

Authors: Proenza, AM Poissonnet, CM Ozata, M Ozen, S Guran, S Palou, A Strosberg, AD

Citation: Am. Proenza et al., Association of sets of alleles of genes encoding beta(3)-adrenoreceptor, uncoupling protein 1 and lipoprotein lipase with increased risk of metaboliccomplications in obesity, INT J OBES, 24(1), 2000, pp. 93-100

Authors: Ural, AU Kaptan, K Avcu, F Guran, S Beyan, C Durmus, O Yalcin, A

Citation: Au. Ural et al., Chronic myelomonocytic leukemia developed 2 years after the onset of immune thrombocytopenic purpura like syndrome, HAEMATOLOGI, 30(3), 2000, pp. 221-224

Authors: Guran, S Tunca, Y Imirzalioglu, N

Citation: S. Guran et al., Hereditary TP53 codon 292 and somatic P16(INK4A) codon 94 mutations in a Li-Fraumeni syndrome family, CANC GENET, 113(2), 1999, pp. 145-151

Authors: Guran, S Pak, I

Citation: S. Guran et I. Pak, Cumulation of TP53 mutations and p16(INK4A)/p15(INK4B) homozygous deletions in human papilloma virus type 16 positive scrotal cancer, CANC GENET, 109(2), 1999, pp. 108-113

Authors: Guran, S Bahce, M Beyan, C Korkmaz, K Yalcin, A

Citation: S. Guran et al., P53, p15(INK4B), p16(INK4A) and p57(KIP2) mutations during the progressionof chronic myeloid leukemia, HAEMATOLOGI, 29(3), 1998, pp. 181-193