학술논문
'학술논문'
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1~10
Academic Journal
Morren, Marie-Anne; Fodstad, Heidi; Brems, Hilde; Bedoni, Nicola; Guenova, Emmanuella; Jacot-Guillarmod, Martine; Busiah, Kanetee; Giuliano, Fabienne; Gilliet, Michel; Atallah, Isis
Journal of Medical Genetics; May2024, Vol. 61 Issue 5, p411-419, 9p
Academic Journal
Bastos, Filipa; Quinodoz, Mathieu; Addor, Marie-Claude; Royer-Bertrand, Beryl; Fodstad, Heidi; Rivolta, Carlo; Poloni, Claudia; Superti-Furga, Andrea; Roulet-Perez, Eliane; Lebon, Sebastien
Academic Journal
Royer‐Bertrand, Beryl; Lebon, Sébastien; Craig, Ailsa; Maeder, Johanna; Mittaz‐Crettol, Laureane; Fodstad, Heidi; Superti‐Furga, Andrea; Good, Jean‐Marc
American Journal of Medical Genetics. Part A; Jun2023, Vol. 191 Issue 6, p1658-1663, 6p
Academic Journal
Lehtonen, Annukka; Fodstad, Heidi; Laitinen-Forsblom, Päivi; Toivonen, Lauri; Kontula, Kimmo; Swan, Heikki
In Heart Rhythm 2007 4(5):603-607
Academic Journal
Paavonen, Kristian J.; Swan, Heikki; Piippo, Kirsi; Laitinen, Päivi; Fodstad, Heidi; Sarna, Seppo; Toivonen, Lauri; Kontula, Kimmo; Viitasalo, Matti
In International Journal of Cardiology 2007 118(2):197-202
Loss-of-function mutations of the K + channel gene KCNJ2 constitute a rare cause of long QT syndrome
Academic Journal
Fodstad, Heidi; Swan, Heikki; Auberson, Muriel; Gautschi, Ivan; Loffing, Johannes; Schild, Laurent; Kontula, Kimmo
In Journal of Molecular and Cellular Cardiology 2004 37(2):593-602
Academic Journal
Kim, Sobin; Shi, Shundi; Bonome, Tomás; Ulz, Michael E.; Edwards, John R.; Fodstad, Heidi; Russo, James J.; Ju, Jingyue
In Analytical Biochemistry 2003 316(2):251-258
Periodical
Aerden, Mio; Denommé-Pichon, Anne-Sophie; Bonneau, Dominique; Bruel, Ange-Line; Delanne, Julian; Gérard, Bénédicte; Mazel, Benoît; Philippe, Christophe; Pinson, Lucile; Prouteau, Clément; Putoux, Audrey; Tran Mau-Them, Frédéric; Viora-Dupont, Éléonore; Vitobello, Antonio; Ziegler, Alban; Piton, Amélie; Isidor, Bertrand; Francannet, Christine; Maillard, Pierre-Yves; Julia, Sophie; Philippe, Anais; Schaefer, Elise; Koene, Saskia; Ruivenkamp, Claudia; Hoffer, Mariette; Legius, Eric; Theunis, Miel; Keren, Boris; Buratti, Julien; Charles, Perrine; Courtin, Thomas; Misra-Isrie, Mala; van Haelst, Mieke; Waisfisz, Quinten; Wieczorek, Dagmar; Schmetz, Ariane; Herget, Theresia; Kortüm, Fanny; Lisfeld, Jasmin; Debray, François-Guillaume; Bramswig, Nuria C.; Atallah, Isis; Fodstad, Heidi; Jouret, Guillaume; Almoguera, Berta; Tahsin-Swafiri, Saoud; Santos-Simarro, Fernando; Palomares-Bralo, Maria; López-González, Vanesa; Kibaek, Maria; Tørring, Pernille M.; Renieri, Alessandra; Bruno, Lucia Pia; Õunap, Katrin; Wojcik, Monica; Hsieh, Tzung-Chien; Krawitz, Peter; Van Esch, Hilde
European Journal of Human Genetics: EJHG; April 2023, Vol. 31 Issue: 4 p461-468, 8p
Academic Journal
Pietilä, Eeva; Fodstad, Heidi; Niskasaari, Elmo; Laitinen, P.äivi J; Swan, Heikki; Savolainen, Markku; Kesäniemi, Y.Antero; Kontula, Kimmo; Huikuri, Heikki V
In Journal of the American College of Cardiology 7 August 2002 40(3):511-514
Homozygous GLI3 variants observed in three unrelated patients presenting with syndromic polydactyly.
Academic Journal
El Mouatani, Ahmed; Van Winckel, Géraldine; Zaafrane‐Khachnaoui, Khaoula; Whalen, Sandra; Achaiaa, Amale; Kaltenbach, Sophie; Superti‐Furga, Andrea; Vekemans, Michel; Fodstad, Heidi; Giuliano, Fabienne; Attie‐Bitach, Tania
American Journal of Medical Genetics. Part A; Dec2021, Vol. 185 Issue 12, p3831-3837, 7p
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제한된 항목
[AR] Fodstad, Heidi
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