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Citation: B. Van Den Bos et al., Automatic scanning with multi-frequency eddy current on multilayered structures, INSIGHT, 43(3), 2001, pp. 163-166

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: Anderlid, BM Sahlen, S Schoumans, J Holmberg, E Ahsgren, I Mortier, G Speleman, F Blennow, E

Citation: Bm. Anderlid et al., Detailed characterization of 12 supernumerary ring chromosomes using micro-FISH and search for uniparental disomy, AM J MED G, 99(3), 2001, pp. 223-233

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: Tsezou, A Kitsiou, S Galla, A Petersen, MB Karadima, G Syrrou, M Sahlen, S Blennow, E

Citation: A. Tsezou et al., Molecular cytogenetic characterization and origin of two de novo duplication 9p cases, AM J MED G, 91(2), 2000, pp. 102-106

Authors: Blennow, E Sahlen, S

Citation: E. Blennow et S. Sahlen, Rescue from the effects of trisomy 13q32 -> qter owing to skewed X inactivation in a der(X)t(X;13) (p21;q32) carrier, J MED GENET, 36(9), 1999, pp. 718-719