MED12 exon 2 mutations in histopathological uterine leiomyoma variants von Mäkinen, Netta, Vahteristo, Pia, Kämpjärvi, Kati, Arola, Johanna, Bützow, Ralf, Aaltonen, Lauri A

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Mutations in Exon 1 Highlight the Role of MED12 in Uterine Leiomyomas von Kämpjärvi, Kati, Park, Min Ju, Mehine, Miika, Kim, Nam Hee, Clark, Alison D., Bützow, Ralf, Böhling, Tom, Böhm, Jan, Mecklin, Jukka-Pekka, Järvinen, Heikki, Tomlinson, Ian P.M., van der Spuy, Zephne M., Sjöberg, Jari, Boyer, Thomas G., Vahteristo, Pia

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MED12 mutations and FH inactivation are mutually exclusive in uterine leiomyomas von Kämpjärvi, Kati, Mäkinen, Netta, Mehine, Miika, Välipakka, Salla, Uimari, Outi, Pitkänen, Esa, Heinonen, Hanna-Riikka, Heikkinen, Tuomas, Tolvanen, Jaana, Ahtikoski, Anne, Frizzell, Norma, Sarvilinna, Nanna, Sjöberg, Jari, Bützow, Ralf, Aaltonen, Lauri A, Vahteristo, Pia

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Somatic MED12 Nonsense Mutation Escapes mRNA Decay and Reveals a Motif Required for Nuclear Entry von Heikkinen, Tuomas, Kämpjärvi, Kati, Keskitalo, Salla, von Nandelstadh, Pernilla, Liu, Xiaonan, Rantanen, Ville, Pitkänen, Esa, Kinnunen, Matias, Kuusanmäki, Heikki, Kontro, Mika, Turunen, Mikko, Mäkinen, Netta, Taipale, Jussi, Heckman, Caroline, Lehti, Kaisa, Mustjoki, Satu, Varjosalo, Markku, Vahteristo, Pia

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Towards Uncovering the Role of Incomplete Penetrance in Maculopathies through Sequencing of 105 Disease-Associated Genes von Hitti-Malin, Rebekkah J, Panneman, Daan M, Corradi, Zelia, Boonen, Erica G M, Astuti, Galuh, Dhaenens, Claire-Marie, Stöhr, Heidi, Weber, Bernhard H F, Sharon, Dror, Banin, Eyal, Karali, Marianthi, Banfi, Sandro, Ben-Yosef, Tamar, Glavač, Damjan, Farrar, G Jane, Ayuso, Carmen, Liskova, Petra, Dudakova, Lubica, Vajter, Marie, Ołdak, Monika, Szaflik, Jacek P, Matynia, Anna, Gorin, Michael B, Kämpjärvi, Kati, Bauwens, Miriam, De Baere, Elfride, Hoyng, Carel B, Li, Catherina H Z, Klaver, Caroline C W, Inglehearn, Chris F, Fujinami, Kaoru, Rivolta, Carlo, Allikmets, Rando, Zernant, Jana, Lee, Winston, Podhajcer, Osvaldo L, Fakin, Ana, Sajovic, Jana, AlTalbishi, Alaa, Valeina, Sandra, Taurina, Gita, Vincent, Andrea L, Roberts, Lisa, Ramesar, Raj, Sartor, Giovanna, Luppi, Elena, Downes, Susan M, van den Born, L Ingeborgh, McLaren, Terri L, De Roach, John N, Lamey, Tina M, Thompson, Jennifer A, Chen, Fred K, Tracewska, Anna M, Kamakari, Smaragda, Sallum, Juliana Maria Ferraz, Bolz, Hanno J, Kayserili, Hülya, Roosing, Susanne, Cremers, Frans P M

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Towards uncovering the role of incomplete penetrance in maculopathies through sequencing of 105 disease-associated genes von Hitti-Malin, Rebekkah J, Panneman, Daan M, Corradi, Zelia, Boonen, Erica G. M, Astuti, Galuh, Dhaenens, Claire-Marie, Stoehr, Heidi, Weber, Bernhard H. F, Sharon, Dror, Banin, Eyal, Karali, Marianthi, Banfi, Sandro, Ben-Yosef, Tamar, Glavac, Damjan, Farrar, G. Jane, Ayuso, Carmen, Liskova, Petra, Dudakova, Lubica, Vajter, Marie, Oldak, Monika, Szaflik, Jacek P, Matynia, Anna, Gorin, Michael B, Kaempjaervi, Kati, Bauwens, Miriam, De Baere, Elfride, Hoyng, Carel B, Li, Catherina H. Z, Klaver, Caroline C. W, Inglehearn, Chris F, Fujinami, Kaoru, Rivolta, Carlo, Allikmets, Rando, Zernant, Jana, Lee, Winston, Podhajcer, Osvaldo L, Fakin, Ana, Sajovic, Jana, Altalbishi, Alaa, Valeina, Sandra, Taurina, Gita, Vincent, Andrea L, Roberts, Lisa, Ramesar, Raj, Sartor, Giovanna, Luppi, Elena, Downes, Susan M, van den Born, L. Ingeborgh, Mclaren, Terri L, De Roach, John N, Lamey, Tina M, Thompson, Jennifer A, Chen, Fred K, Tracewska, Anna M, Kamakari, Smaragda, Sallum, Juliana Maria Ferraz, Bolz, Hanno J, Kayserili, Huelya, Roosing, Susanne, Cremers, Frans P. M

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