The Finnish disease heritage III: the individual diseases von NORIO, Reijo

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Finnish Disease Heritage II: population prehistory and genetic roots of Finns von NORIO, Reijo

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Comparative PRKAR1A Genotype-Phenotype Analyses in Humans with Carney Complex and prkar1a Haploinsufficient Mice von Veugelers, Mark, Wilkes, David, Burton, Kimberly, McDermott, Deborah A., Song, Yan, Goldstein, Marsha M., La Perle, Krista, Vaughan, Carl J., O'Hagan, Art, Bennett, Kenneth R., Meyer, Beat J., Legius, Eric, Karttunen, Mervi, Norio, Reijo, Kaariainen, Helena, Lavyne, Michael, Neau, Jean-Philippe, Richter, Gert, Kirali, Kaan, Farnsworth, Alan, Stapleton, Karen, Morelli, Peter, Takanashi, Yoshinori, Bamforth, John-Steven, Eitelberger, Franz, Noszian, Irene, Manfroi, Waldimiro, Powers, James, Mochizuki, Yoshihiko, Imai, Tsuneo, Gary T. C. Ko, Driscoll, Deborah A., Goldmuntz, Elizabeth, Edelberg, Jay M., Collins, Amanda, Eccles, Diana, Irvine, Alan D., McKnight, G. Stanley, Basson, Craig T., Taylor, Susan S.

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Finnish Disease Heritage I: characteristics, causes, background von NORIO, Reijo

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Mutations in the Gene Encoding Cystatin B in Progressive Myoclonus Epilepsy (EPM1) von Pennacchio, Len A., Lehesjoki, Anna-Elina, Stone, Nancy E., Willour, Virginia L., Virtaneva, Kimmo, Miao, Jinmin, D'Amato, Elena, Ramirez, Lucia, Faham, Malek, Koskiniemi, Marjaleena, Warrington, Janet A., Norio, Reijo, de la Chapelle, Albert, Cox, David R., Myers, Richard M.

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Finnish Disease Heritage I von Norio, Reijo

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Unstable minisatellite expansion causing recessively inherited myoclonus epilepsy, EPM1 von Virtaneva, Kimmo, D'Amato, Elena, Miao, Jinmin, Koskiniemi, Marjaleena, Norio, Reijo, Avanzini, Giuliano, Franceschetti, Silvana, Michelucci, Roberto, Tassinari, Carlo A., Omer, Salah, Pennacchio, Len A., Myers, Richard M., Dieguez-Lucena, José L., Krahe, Ralf, Chapelle, Albert de la, Lehesjoki, Anna-Elina

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Cohen Syndrome Is Caused by Mutations in a Novel Gene, COH1, Encoding a Transmembrane Protein with a Presumed Role in Vesicle-Mediated Sorting and Intracellular Protein Transport von Kolehmainen, Juha, Black, Graeme C.M., Saarinen, Anne, Chandler, Kate, Clayton-Smith, Jill, Träskelin, Ann-Liz, Perveen, Rahat, Kivitie-Kallio, Satu, Norio, Reijo, Warburg, Mette, Fryns, Jean-Pierre, Chapelle, Albert de la, Lehesjoki, Anna-Elina

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Localization of a Gene for Progressive Myoclonus Epilepsy to Chromosome 21q22 von LEHESIOKI, A.-E, KOSKINIEMI, M, SISTONEN, P, JINMIN MIAO, HASTBACKA, J, NORIO, R, DE LA CHAPELLE, A

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Granulocytopenia in Cohen syndrome von Kivitie‐Kallio, Satu, Rajantie, Jukka, Juvonen, Eeva, Norio, Reijo

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Intestinal cancer in patients with a germline mutation in the down-regulated in adenoma (DRA) gene von HEMMINKI, A, HÖGLUND, P, PUKKALA, E, SALOVAARA, R, JÄRVINEN, H, NORIO, R, AALTONEN, L. A

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The Finnish disease heritage von Reijo Norio, Markku Löytönen

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Delineation of Cohen Syndrome Following a Large-Scale Genotype-Phenotype Screen von Kolehmainen, Juha, Wilkinson, Robert, Lehesjoki, Anna-Elina, Chandler, Kate, Kivitie-Kallio, Satu, Clayton-Smith, Jill, Träskelin, Ann-Liz, Waris, Laura, Saarinen, Anne, Khan, Jabbar, Gross-Tsur, Varda, Traboulsi, Elias I., Warburg, Mette, Fryns, Jean-Pierre, Norio, Reijo, C. M. Black, Graeme, D. C. Manson, Forbes

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Ophthalmologic findings in cohen syndrome: A long-term follow-up von Kivitie-Kallio, Satu, Summanen, Paula, Raitta, Christina, Norio, Reijo

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The Finnish disease heritage as a product of the population structure von Norio, Reijo

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Mechanisms of Myopia in Cohen Syndrome Mapped to Chromosome 8q22 von Summanen, Paula, Kivitie-Kallio, Satu, Norio, Reijo, Raitta, Christina, Kivela, Tero

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The desmoid tumor. III. A biochemical and genetic analysis von Häyry, P, Reitamo, J J, Vihko, R, Jänne, O, Scheinin, T M, Tötterman, S, Ahonen, J, Norio, R, Alanko, A

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Ophthalmologic findings in cohen syndrome von Kivitie-Kallio, Satu, Summanen, Paula, Raitta, Christina, Norio, Reijo

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Cohen syndrome gene assigned to the long arm of chromosome 8 by linkage analysis von Tahvanainen, Esa, Norio, Reijo, Karila, Elvi, Ranta, Susanna, Weissenbach, Jean, Sistonen, Pertti, de la Chapelle, Albert

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Intimal thickening of the coronary arteries in infants in relation to family history of coronary artery disease von KAPRIO, J, NORIO, R, PESONEN, E, SARNA, S

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