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Results: 1-7 |
Results: 7
Genetic analysis in Finnish families with inflammatory bowel disease supports linkage to chromosome 3p21
Authors: Paavola, P Helio, T Kiuru, M Halme, L Turunen, U Terwilliger, J Karvonen, AL Julkunen, R Niemela, S Nurmi, H Farkkila, M Kontula, K
Citation: P. Paavola et al., Genetic analysis in Finnish families with inflammatory bowel disease supports linkage to chromosome 3p21, EUR J HUM G, 9(5), 2001, pp. 328-334
Comprehensive copy number and gene expression profiling of the 17q23 amplicon in human breast cancer
Authors: Monni, O Barlund, M Mousses, S Kononen, J Sauter, G Heiskanen, M Paavola, P Avela, K Chen, YD Bittner, ML Kallioniemi, A
Citation: O. Monni et al., Comprehensive copy number and gene expression profiling of the 17q23 amplicon in human breast cancer, P NAS US, 98(10), 2001, pp. 5711-5716
High-resolution physical and genetic mapping of the critical region for Meckel syndrome and Mulibrey Nanism on chromosome 17q22-q23
Authors: Paavola, P Avela, K Horelli-Kuitunen, N Barlund, M Kallioniemi, A Idanheimo, N Kyttala, M de la Chapelle, A Palotie, A Lehesjoki, AE Peltonen, L
Citation: P. Paavola et al., High-resolution physical and genetic mapping of the critical region for Meckel syndrome and Mulibrey Nanism on chromosome 17q22-q23, GENOME RES, 9(3), 1999, pp. 267-276
Characterization of a novel gene, PNUTL2, on human chromosome 17q22-q23 and its exclusion as the Meckel syndrome gene
Authors: Paavola, P Horelli-Kuitunen, N Palotie, A Peltonen, L
Citation: P. Paavola et al., Characterization of a novel gene, PNUTL2, on human chromosome 17q22-q23 and its exclusion as the Meckel syndrome gene, GENOMICS, 55(1), 1999, pp. 122-125
Characterization of the lysinuric protein intolerance (LPI) region within T-cell receptor alpha/delta gene cluster on chromosome site 14q11
Authors: Lauteala, T Mykkanen, J Horelli-Kuitunen, N Aaltonen, J Paavola, P Savontaus, ML Simell, O Aula, P
Citation: T. Lauteala et al., Characterization of the lysinuric protein intolerance (LPI) region within T-cell receptor alpha/delta gene cluster on chromosome site 14q11, HEREDITAS, 130(1), 1999, pp. 19-24
Assignment of the locus for hydrolethalus syndrome to a highly restricted region on 11q23-25
Authors: Visapaa, I Salonen, R Varilo, T Paavola, P Peltonen, L
Citation: I. Visapaa et al., Assignment of the locus for hydrolethalus syndrome to a highly restricted region on 11q23-25, AM J HU GEN, 65(4), 1999, pp. 1086-1095
Molecular cytogenetic mapping of 24 CEPH YACs and 24 gene-specific large insert probes to chromosome 17
Authors: Barlund, M Nupponen, NN Karhu, R Tanner, MM Paavola, P Kallioniemi, OP Kallioniemi, A
Citation: M. Barlund et al., Molecular cytogenetic mapping of 24 CEPH YACs and 24 gene-specific large insert probes to chromosome 17, CYTOG C GEN, 82(3-4), 1998, pp. 189-191
Risultati: 1-7 |