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:
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
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