Authors: Bruder, CEG Hirvela, C Tapia-Paez, I Fransson, I Segraves, R Hamilton, G Zhang, XX Evans, DG Wallace, AJ Baser, ME Zucman-Rossi, J Hergersberg, M Boltshauser, E Papi, L Rouleau, GA Poptodorov, G Jordanova, A Rask-Andersen, H Kluwe, L Mautner, V Sainio, M Hung, G Mathiesen, T Moller, C Pulst, SM Harder, H Heiberg, A Honda, M Miimura, M Sahlen, S Blennow, E Albertson, DG Pinkel, D Dumanski, JP

Citation: Ceg. Bruder et al., High resolution deletion analysis of constitutional DNA from neurofibromatosis type 2 (NF2) patients using microarray-CGH, HUM MOL GEN, 10(3), 2001, pp. 271-282

Authors: Grigelioniene, G Schoumans, J Neumeyer, L Ivarsson, SA Eklof, O Enkvist, O Tordai, P Fosdal, I Myhre, AG Westphal, O Nilsson, NO Elfving, M Ellis, I Anderlid, BM Fransson, I Tapia-Paez, I Nordenskjold, M Hagenas, L Dumanski, JP

Citation: G. Grigelioniene et al., Analysis of short stature homeobox-containing gene (SHOX) and auxological phenotype in dyschondrosteosis and isolated Madelung deformity, HUM GENET, 109(5), 2001, pp. 551-558

Authors: Tapia-Paez, I Kost-Alimova, M Hu, P Roe, BA Blennow, E Fedorova, L Imreh, S Dumanski, JP

Citation: I. Tapia-paez et al., The position of t(11;22)(q23;q11) constitutional translocation breakpoint is conserved among its carriers, HUM GENET, 109(2), 2001, pp. 167-177

Authors: Tapia-Paez, I O'Brien, KP Kost-Alimova, M Sahlen, S Kedra, D Bruder, CEG Andersson, B Roe, BA Hu, P Imreh, S Blennow, E Dumanski, JP

Citation: I. Tapia-paez et al., Fine mapping of the constitutional translocation t(11;22)(q23;q11), HUM GENET, 106(5), 2000, pp. 506-516

Authors: O'Brien, KP Tapia-Paez, I Stahle-Backdahl, M Kedra, D Dumanski, JP

Citation: Kp. O'Brien et al., Characterization of five novel human genes in the 11q13-q22 region, BIOC BIOP R, 273(1), 2000, pp. 90-94