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Results: 1-9 |
Results: 9
Involvement of BRCA1 and BRCA2 in breast cancer in a Western Finnish sub-population
Authors: Paakkonen, K Sauramo, S Sarantaus, L Vahteristo, P Hartikainen, A Vehmanen, P Ignatius, J Ollikainen, V Kaariainen, H Vauramo, E Nevanlinna, H Krahe, R Holli, K Kere, J
Citation: K. Paakkonen et al., Involvement of BRCA1 and BRCA2 in breast cancer in a Western Finnish sub-population, GENET EPID, 20(2), 2001, pp. 239-246
QCD phase transition in the inhomogeneous universe
Authors: Ignatius, J Schwarz, DJ
Citation: J. Ignatius et Dj. Schwarz, QCD phase transition in the inhomogeneous universe, PHYS REV L, 86(11), 2001, pp. 2216-2219
Evidence for a common Spinocerebellar ataxia type 7 (SCA7) founder mutation in Scandinavia
Authors: Jonasson, J Juvonen, V Sistonen, P Ignatius, J Johansson, D Bjorck, EJ Wahlstrom, J Melberg, A Holmgren, G Forsgren, L Holmberg, M
Citation: J. Jonasson et al., Evidence for a common Spinocerebellar ataxia type 7 (SCA7) founder mutation in Scandinavia, EUR J HUM G, 8(12), 2000, pp. 918-922
Capacitive ultrasonic transducer with net backplate
Authors: Mattila, P Stor-Pellinen, J Ignatius, J Hietanen, J Luukkala, M
Citation: P. Mattila et al., Capacitive ultrasonic transducer with net backplate, MEAS SCI T, 11(8), 2000, pp. 1119-1125
Familiar perisylvian polymicrogyria: A new familial syndrome of cortical maldevelopment
Authors: Guerreiro, MM Andermann, E Guerrini, R Dobyns, WB Kuzniecky, R Silver, K Van Bogaert, P Gillain, C David, P Ambrosetto, G Rosati, A Bartolomei, F Parmeggiani, A Paetau, R Salonen, O Ignatius, J Borgatti, R Zucca, C Bastos, AC Palmini, A Fernandes, W Montenegro, MA Cendes, F Andermann, F
Citation: Mm. Guerreiro et al., Familiar perisylvian polymicrogyria: A new familial syndrome of cortical maldevelopment, ANN NEUROL, 48(1), 2000, pp. 39-48
Smith-Lemli-Opitz syndrome and other sterol disorders among Finns with developmental disabilities
Authors: Nissinen, MJ Gylling, H Kaski, M Tammisto, P Mieskonen, S Ignatius, J Miettinen, TA
Citation: Mj. Nissinen et al., Smith-Lemli-Opitz syndrome and other sterol disorders among Finns with developmental disabilities, J LA CL MED, 136(6), 2000, pp. 457-467
Assignment of a novel locus for autosomal recessive congenital ichthyosis chromosome 19p13.1-p13.2
Authors: Virolainen, E Wessman, M Hovatta, I Niemi, KM Ignatius, J Kere, J Peltonen, L Palotie, A
Citation: E. Virolainen et al., Assignment of a novel locus for autosomal recessive congenital ichthyosis chromosome 19p13.1-p13.2, AM J HU GEN, 66(3), 2000, pp. 1132-1137
Clinical and morphological correlations for transglutaminase 1 gene mutations in autosomal recessive congenital ichthyosis
Authors: Laiho, E Niemi, KM Ignatius, J Kere, J Palotie, A Saarialho-Kere, U
Citation: E. Laiho et al., Clinical and morphological correlations for transglutaminase 1 gene mutations in autosomal recessive congenital ichthyosis, EUR J HUM G, 7(6), 1999, pp. 625-632
Clinical spectrum and diagnostic difficulties of infantile ponto-cerebellar hypoplasia type 1
Authors: Muntoni, F Goodwin, F Sewry, C Cox, P Cowan, F Airaksinen, E Patel, S Ignatius, J Dubowitz, V
Citation: F. Muntoni et al., Clinical spectrum and diagnostic difficulties of infantile ponto-cerebellar hypoplasia type 1, NEUROPEDIAT, 30(5), 1999, pp. 243-248
Risultati: 1-9 |