Microsatellite marker analysis in screening for hereditary nonpolyposis colorectal cancer (HNPCC) von LOUKOLA, Anu, EKLIN, Katja, LAIHO, Päivi, SALOVAARA, Reijo, KRISTO, Paula, JÄRVINEN, Heikki, MECKLIN, Jukka-Pekka, LAUNONEN, Virpi, AALTONEN, Lauri A

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Frequent loss of SMAD4/DPC4 protein in colorectal cancers von Salovaara, R, Roth, S, Loukola, A, Launonen, V, Sistonen, P, Avizienyte, E, Kristo, P, Järvinen, H, Souchelnytskyi, S, Sarlomo-Rikala, M, Aaltonen, L A

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Molecular Screening for Hereditary Nonpolyposis Colorectal Cancer: A Prospective, Population-Based Study von PERCESEPE, Antonio, BORGHI, Francesca, RONCUCCI, Luca, BENATTI, Piero, VIEL, Alessandra, GENUARDI, Maurizio, MARRA, Giancarlo, KRISTO, Paula, PELTOMÄKI, Paivi, PONZ DE LEON, Maurizio, MENIGATTI, Mirco, LOSI, Lorena, FORONI, Moira, DI GREGORIO, Carmela, ROSSI, Giuseppina, PEDRONI, Monica, SALA, Elisa, VACCINA, Fabiana

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Four novel mutations in the OFD1 (Cxorf5) gene in Finnish patients with oral-facial-digital syndrome 1 von Rakkolainen, A, Ala-Mello, S, Kristo, P, Orpana, A, Järvelä, I

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Incidence of Hereditary Nonpolyposis Colorectal Cancer and the Feasibility of Molecular Screening for the Disease von Aaltonen, Lauri A, Salovaara, Reijo, Kristo, Paula, Canzian, Federico, Hemminki, Akseli, Peltomäki, Päivi, Chadwick, Robert B, Kääriäinen, Helena, Eskelinen, Matti, Järvinen, Heikki, Mecklin, Jukka-Pekka, de la Chapelle, Albert, Percesepe, Antonio, Ahtola, Heikki, Härkönen, Niilo, Julkunen, Risto, Kangas, Eero, Ojala, Seppo, Tulikoura, Jukka, Valkamo, Erkki

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Population-Based Molecular Detection of Hereditary Nonpolyposis Colorectal Cancer von Salovaara, R, Loukola, A, Kristo, P, Kääriäinen, H, Ahtola, H, Eskelinen, M, Härkönen, N, Julkunen, R, Kangas, E, Ojala, S, Tulikoura, J, Valkamo, E, Järvinen, H, Mecklin, J P, Aaltonen, L A, de la Chapelle, A

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A serine/threonine kinase gene defective in Peutz-Jeghers syndrome von Aaltonen, Lauri A, Hemminki, Akseli, Markie, David, Tomlinson, Ian, Avizienyte, Egle, Roth, Stina, Loukola, Anu, Bignell, Graham, Warren, William, Aminoff, Maria, Höglund, Pia, Järvinen, Heikki, Kristo, Paula, Pelin, Katarina, Ridanpää, Maaret, Salovaara, Reijo, Toro, Tumi, Bodmer, Walter, Olschwang, Sylviane, Olsen, Anne S, Stratton, Michael R, de la Chapelle, Albert

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Small N‐Terminal Deletion by Splicing in Cerebellar α6 Subunit Abolishes GABAA Receptor Function von Korpi, E. R., Kuner, T., Kristo, P., Köhler, M., Herb, A., Lüddens, H., Seeburg, P. H.

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Mutation sharing, predominant involvement of the MLH1 gene and description of four novel mutations in hereditary nonpolyposis colorectal cancer. Mutations in brief no. 144. Online von Holmberg, M, Kristo, P, Chadwicks, R B, Mecklin, J P, Järvinen, H, de la Chapelle, A, Nyström-Lahti, M, Peltomäki, P

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Evidence for two molecular steps in the pathogenesis of myeloid disorders associated with deletion of chromosome 7 long arm von KIURU-KUHLEFELT, S, KRISTO, P, RUUTU, T, KNUUTILA, S, KERE, J

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Semiautomated assessment of loss of heterozygosity and replication error in tumors von CANZIAN, F, SALOVAARA, R, HEMMINKI, A, KRISTO, P, CHADWICK, R. B, AALTONEN, L. A, DE LA CHAPELLE, A

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Protein purification, and cloning and characterization of the cDNA and gene for xylose isomerase of barley von Kristo, P, Saarelainen, R, Fagerstrom, R, Aho, S, Korhola, M

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Founding mutations and Alu-mediated recombination in hereditary colon cancer von Nyström-Lahti, Minna, Kristo, Paula, Nicolaides, Nicholas C, Chang, Sheng-Yung, Aaltonen, Lauri A, Moisio, Anu-Liisa, Järvinen, Heikki J, Mecklin, Jukka-Pekka, Kinzler, Kenneth W, Vogelstein, Bert, De La Chapelle, Albert, Peltomäki, Päivi

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The role of TIGR and OPTN in Finnish glaucoma families: a clinical and molecular genetic study von Forsman, Eva, Lemmelä, Susanna, Varilo, Teppo, Kristo, Paula, Forsius, Henrik, Sankila, Eeva-Marja, Järvelä, Irma

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A missense mutation in the BRCA2 gene in three siblings with ovarian cancer von Roth, S, Kristo, P, Auranen, A, Shayehgi, M, Seal, S, Collins, N, Barfoot, R, Rahman, N, Klemi, PJ, Grénman, S, Sarantaus, L, Nevanlinna, H, Butzow, R, Ashworth, A, Stratton, MR, Aaltonen, LA

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Microsatellite Instability in Adenomas as a Marker for Hereditary Nonpolyposis Colorectal Cancer von Loukola, Anu, Salovaara, Reijo, Kristo, Paula, Moisio, Anu-Liisa, Kääriäinen, Helena, Ahtola, Heikki, Eskelinen, Matti, Härkönen, Niilo, Julkunen, Risto, Kangas, Eero, Ojala, Seppo, Tulikoura, Jukka, Valkamo, Erkki, Järvinen, Heikki, Mecklin, Jukka-Pekka, de la Chapelle, Albert, Aaltonen, Lauri A.

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Genetic Screening for Maternal Uniparental Disomy of Chromosome 7 in Prenatal and Postnatal Growth Retardation of Unknown Cause von Hannula, Katariina, Lipsanen-Nyman, Marita, Kristo, Paula, Kaitila, Ilkka, Simola, Kalle O. J, Lenko, Hanna Liisa, Tapanainen, Paivi, Holmberg, Christer, Kere, Juha

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Molecular cloning of the chicken avidin cDNA von GOPE, M. L, KEINANEN, R. A, KRISTO, P. A, CONNEELY, O. M, BEATTIE, W. G, ZARUCKI-SCHULZ, T, O'MALLEY, B. W, KULOMAA, M. S

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Mismatch repair genes and mononucleotide tracts as mutation targets in colorectal tumors with different degrees of microsatellite instability von PERCESEPE, A, KRISTO, P, AALTONEN, L. A, PONZ DE LEON, M, DE LA CHAPELLE, A, PELTOMÄKI, P

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Ultrastructural and Chromosomal Studies on Manganese Superoxide Dismutase in Malignant Mesothelioma von Kinnula, Vuokko L, Torkkeli, Tuula, Kristo, Paula, Sormunen, Raija, Soini, Ylermi, Paakko, Paavo, Ollikainen, Tiina, Kahlos, Katriina, Hirvonen, Ari, Knuutila, Sakari

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