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