학술논문
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'학술논문'
에서 검색결과 222건 | 목록
1~20
Academic Journal
Anderson, Eric N. ; Drukewitz, Stephan ; Kour, Sukhleen ; Chimata, Anuradha V. ; Rajan, Deepa S. ; Schönnagel, Senta ; Stals, Karen L. ; Donnelly, Deirdre ; O'Sullivan, Siobhan ; Mantovani, John F. ; Tan, Tiong Y. ; Stark, Zornitza ; Zacher, Pia ; Chatron, Nicolas ; Monin, Pauline ; Drunat, Severine ; Vial, Yoann ; Latypova, Xenia ; Levy, Jonathan ; Verloes, Alain ; Carter, Jennefer N. ; Bonner, Devon E. ; Shankar, Suma P. ; Bernstein, Jonathan A. ; Cohen, Julie S. ; Comi, Anne ; Carere, Deanna Alexis ; Dyer, Lisa M. ; Mullegama, Sureni V. ; Sanchez-Lara, Pedro A. ; Grand, Katheryn ; Kim, Hyung-Goo ; Ben-Mahmoud, Afif ; Gospe, Sidney M., Jr. ; Belles, Rebecca S. ; Bellus, Gary ; Lichtenbelt, Klaske D. ; Oegema, Renske ; Rauch, Anita ; Ivanovski, Ivan ; Mau-Them, Frederic Tran ; Garde, Aurore ; Rabin, Rachel ; Pappas, John ; Bley, Annette E. ; Bredow, Janna ; Wagner, Timo ; Decker, Eva ; Bergmann, Carsten ; Domenach, Louis ; Margot, Henri ; Lemke, Johannes R. ; Abou Jamra, Rami ; Hentschel, Julia ; Mefford, Heather ; Singh, Amit ; Pandey, Udai Bhan ; Platzer, Konrad
In The American Journal of Human Genetics 8 January 2026 113(1):100-116
Academic Journal
Ferreira, Elise A. ; Hofstede, Floris C. ; Haijes-Siepel, Hanneke A. ; Lichtenbelt, Klaske D. ; Pistorius, Lou ; de Sain-van der Velden, Monique G.M. ; Nikkels, Peter G.J. ; Lequin, Maarten H. ; de Vries, Linda S. ; van der Crabben, Saskia N. ; van Hasselt, Peter M.
In Genetics in Medicine Open 2024 2
Academic Journal
Severijns, Yil; de Vries, Hein; Tan-Sindhunata, Gita; Stuurman, Kyra; Ottenheim, Cecile; Lichtenbelt, Klaske; van Kuijk, Sander; Joosten, Sara; Houwink, Elisa J. F.; Crutzen, Rik; Corsten-Janssen, Nicole; Bijlsma, Emilia; de Die-Smulders, Christine; van Osch, Liesbeth
Health Psychology Bulletin. April 19, 2023, Vol. 7 Issue 1, p17, 10 p.
Academic Journal
Heesterbeek, Catharina J.; Aukema, Sietse M.; Galjaard, Robert-Jan H.; Boon, Elles M. J.; Srebniak, Malgorzata I.; Bouman, Katelijne; Faas, Brigitte H. W.; Govaerts, Lutgarde C. P.; Hoffer, Mariëtte J. V.; den Hollander, Nicolette S.; Lichtenbelt, Klaske D.; van Maarle, Merel C.; van Prooyen Schuurman, Lisanne; van Rij, Maartje C.; Schuring-Blom, G. Heleen; Stevens, Servi J. C.; Tan-Sindhunata, Gita; Zamani Esteki, Masoud; de Die-Smulders, Christine E. M.; Tjan-Heijnen, Vivianne C. G.; Henneman, Lidewij; Sistermans, Erik A.; MacVille, Merryn V. E.; Polstra, A.; Voorhoeve, E.; Zelderen-Bhola, S. L.; Lombardi, M. P. R.; Bakker, I. M. C.; Bradley, E. J.; Louwerens-Zintel, C.; Smit, M.; van der Meij, K.; Meij, H.; Bax, C. J.; Pajkrt, E.; Linskens, I. H.; Martin, L.; Gitsels-van der Wal, J. T.; van Opstal, D.; Sarquis Jehee, F. M.; Hollink, I. H. I. M.; Sleutels, F.; de Valk, W.; Deelen, W. H.; Joosten, A. M. S.; Diderich, K. E. M.; Redeker, M. E.; Go, A. T. J. I.; Knapen, M. F. C. M.; Galjaard, S.; Prinsen, A. K. E.; Braat, A. P. G.; Verweij, E. J. T.; Haak, M. C.; van der Wijngaard, A.; Houben, L. H.; van Esch-Lennarts, M. A. A.; Hamers, L.; Jetten, A. G. P.; Ghesquiere, S. A. I.; de Koning, B.; Brunner, H.; Pieters, M. J.; Coumans, A. B. C.; Smeets, D. F. C. M.; Westra, D.; Weiss, M. M.; Derks-Prinsen, I.; Feenstra, I.; Sikkel, E.; Suijkerbuijk, R. F.; Sikkema-Raddatz, B.; van Langen, I. M.; Duin, L. K.; Bekker, M. N.; van der Ven, A. J. E. M.; van Vliet-Lachotzki, E.; Pot, J.; van't Padje, S.
Dutch NIPT Consortium 2022, 'Noninvasive Prenatal Test Results Indicative of Maternal Malignancies : A Nationwide Genetic and Clinical Follow-Up Study', Journal of clinical oncology : official journal of the American Society of Clinical Oncology, vol. 40, no. 22, JCO.21.02260, pp. 2426-2435. https://doi.org/10.1200/JCO.21.02260
American Journal of Clinical Oncology, 40, 22, pp. 2426-2435
American Journal of Clinical Oncology, 40, 22, pp. 2426-2435
Academic Journal
Olde Keizer, Richelle A. C. M.; Marouane, Abderrahim; Kerstjens-Frederikse, Wilhelmina S.; Deden, A. Chantal; Lichtenbelt, Klaske D.; Jonckers, Tinneke; Vervoorn, Marieke; Vreeburg, Maaike; Henneman, Lidewij; de Vries, Linda S.; Sinke, Richard J.; Pfundt, Rolph; Stevens, Servi J. C.; Andriessen, Peter; van Lingen, Richard A.; Nelen, Marcel; Scheffer, Hans; Stemkens, Daphne; Oosterwijk, Cor; van Amstel, Hans Kristian Ploos; de Boode, Willem P.; van Zelst-Stams, Wendy A. G.; Frederix, Geert W. J.; Vissers, Lisenka E. L. M.
European Journal of Pediatrics. :1-10
Academic Journal
van Prooyen Schuurman, Lisanne ; Sistermans, Erik A. ; Van Opstal, Diane ; Henneman, Lidewij ; Bekker, Mireille N. ; Bax, Caroline J. ; Pieters, Mijntje J. ; Bouman, Katelijne ; de Munnik, Sonja ; den Hollander, Nicolette S. ; Diderich, Karin E.M. ; Faas, Brigitte H.W. ; Feenstra, Ilse ; Go, Attie T.J.I. ; Hoffer, Mariëtte J.V. ; Joosten, Marieke ; Komdeur, Fenne L. ; Lichtenbelt, Klaske D. ; Lombardi, Maria P. ; Polak, Marike G. ; Jehee, Fernanda S. ; Schuring-Blom, Heleen ; Stevens, Servi J.C. ; Srebniak, Malgorzata I. ; Suijkerbuijk, Ron F. ; Tan-Sindhunata, Gita M. ; van der Meij, Karuna R.M. ; van Maarle, Merel C. ; Vernimmen, Vivian ; van Zelderen-Bhola, Shama L. ; van Ravesteyn, Nicolien T. ; Knapen, Maarten F.C.M. ; Macville, Merryn V.E. ; Galjaard, Robert-Jan H.
In The American Journal of Human Genetics 2 June 2022 109(6):1140-1152
Academic Journal
Lehalle, Daphné; Vabres, Pierre; Sorlin, Arthur; Bierhals, Tatjana; Avila, Magali; Carmignac, Virginie; Chevarin, Martin; Torti, Erin; Abe, Yuichi; Bartolomaeus, Tobias; Clayton-Smith, Jill; Cogné, Benjamin; Cusco, Ivon; Duplomb, Laurence; de Bont, Eveline; Duffourd, Yannis; Duijkers, Floor; Elpeleg, Orly; Fattal, Aviva; Geneviève, David; Guillen Sacoto, Maria; Guimier, Anne; Harris, David; Hempel, Maja; Isidor, Bertrand; Jouan, Thibaud; Kuentz, Paul; Koshimizu, Eriko; Lichtenbelt, Klaske; Loik Ramey, Valerie; Maik, Miriam; Miyakate, Sakoto; Murakami, Yoshiko; Pasquier, Laurent; Pedro, Helio; Simone, Laurie; Sondergaard-Schatz, Krista; St-Onge, Judith; Thevenon, Julien; Valenzuela, Irene; Abou Jamra, Rami; van Gassen, Koen; van Haelst, Mieke; van Koningsbruggen, Silvana; Verdura, Edgard; Whelan Habela, Christa; Zacher, Pia; Rivière, Jean-Baptiste; Thauvin-Robinet, Christel; Betschinger, Joerg; Faivre, Laurence
Lehalle, D, Vabres, P, Sorlin, A, Bierhals, T, Avila, M, Carmignac, V, Chevarin, M, Torti, E, Abe, Y, Bartolomaeus, T, Clayton-Smith, J, Cogné, B, Cusco, I, Duplomb, L, De Bont, E, Duffourd, Y, Duijkers, F, Elpeleg, O, Fattal, A, Geneviève, D, Guillen Sacoto, M J, Guimier, A, Harris, D J, Hempel, M, Isidor, B, Jouan, T, Kuentz, P, Koshimizu, E, Lichtenbelt , K, Loik Ramey, V, Maik, M, Miyakate, S, Murakami, Y, Pasquier, L, Pedro, H, Simone, L, Sondergaard-Schatz, K, St-Onge, J, Thevenon, J, Valenzuela, I, Abou Jamra, R, Van Gassen, K, Van Haelst, M M, Van Koningsbruggen, S, Verdura, E, Whelan Habela, C, Zacher, P, Rivière, J B, Thauvin-Robinet, C, Betschinger, J & Faivre, L 2020, 'De novo mutations in the X-linked TFE3 gene cause intellectual disability with pigmentary mosaicism and storage disorder-like features', Journal of Medical Genetics, vol. 57, no. 12, 106508, pp. 808-819. https://doi.org/10.1136/jmedgenet-2019-106508
Academic Journal
van der Meij, Karuna R M; Sistermans, Erik A; Macville, Merryn V E; Stevens, Servi J C; Bax, Caroline J; Bekker, Mireille N; Bilardo, Caterina M; Boon, Elles M J; Boter, Marjan; Diderich, Karin E M; de Die-Smulders, Christine E M; Duin, Leonie K; Faas, Brigitte H W; Feenstra, Ilse; Haak, Monique C; Hoffer, Mariëtte J V; den Hollander, Nicolette S; Hollink, Iris H I M; Jehee, Fernanda S; Knapen, Maarten F C M; Kooper, Angelique J A; van Langen, Irene M; Lichtenbelt, Klaske D; Linskens, Ingeborg H; van Maarle, Merel C; Oepkes, Dick; Pieters, Mijntje J; Schuring-Blom, G Heleen; Sikkel, Esther; Sikkema-Raddatz, Birgit; Smeets, Dominique F C M; Srebniak, Malgorzata I; Suijkerbuijk, Ron F; Tan-Sindhunata, Gita M; van der Ven, A Jeanine E M; van Zelderen-Bhola, Shama L; Henneman, Lidewij; Galjaard, Robert-Jan H; Van Opstal, Diane; Weiss, Marjan M
van der Meij, K R M, Sistermans, E A, Macville, M V E, Stevens, S J C, Bax, C J, Bekker, M N, Bilardo, C M, Boon, E M J, Boter, M, Diderich, K E M, de Die-Smulders, C E M, Duin, L K, Faas, B H W, Feenstra, I, Haak, M C, Hoffer, M J V, den Hollander, N S, Hollink, I H I M, Jehee, F S, Knapen, M F C M, Kooper, A J A, van Langen, I M, Lichtenbelt , K D, Linskens, I H, van Maarle, M C, Oepkes, D, Pieters, M J, Schuring-Blom, G H, Sikkel, E, Sikkema-Raddatz, B, Smeets, D F C M, Srebniak, M I, Suijkerbuijk, R F, Tan-Sindhunata, G M, van der Ven, A J E M, van Zelderen-Bhola, S L, Henneman, L, Galjaard, R J H, Van Opstal, D, Weiss, M M & The Dutch NIPT Consortium 2019, 'TRIDENT-2 : National Implementation of Genome-wide Non-invasive Prenatal Testing as a First-Tier Screening Test in the Netherlands', American journal of human genetics, vol. 105, no. 6, pp. 1091-1101. https://doi.org/10.1016/j.ajhg.2019.10.005
American Journal of Human Genetics, 105, 6, pp. 1091-1101
American Journal of Human Genetics, 105, 6, pp. 1091-1101
Academic Journal
Konrad, Enrico D.H.; Nardini, Niels; Caliebe, Almuth; Nagel, Inga; Young, Dana; Horvath, Gabriella; Santoro, Stephanie L.; Shuss, Christine; Ziegler, Alban; Bonneau, Dominique; Kempers, Marlies; Pfundt, Rolph; Legius, Eric; Bouman, Arjan; Stuurman, Kyra E.; Ounap, Katrin; Pajusalu, Sander; Wojcik, Monica H.; Vasileiou, Georgia; Le Guyader, Gwenael; Schnelle, Hege M.; Berland, Siren; Zonneveld-Huijssoon, Evelien; Kersten, Simone; Gupta, Aditi; Blackburn, Patrick R.; Ellingson, Marissa S.; Ferber, Matthew J.; Dhamija, Radhika; Klee, Eric W.; McEntagart, Meriel; Lichtenbelt, Klaske D.; Kenney, Amy; Vergano, Samantha A.; Abou Jamra, Rami; Platzer, Konrad; Pierpont, Mary Ella; Khattar, Divya; Hopkin, Robert J.; Martin, Richard J.; Jongmans, Marjolijn C.J.; Chang, Vivian Y.; Martinez-Agosto, Julian A.; Kuismin, Outi; Kurki, Mitja; Pietilainen, Olli; Palotie, Aarno; Maarup, Timothy J.; Johnson, Diana S.; Pedersen, Katja Venborg; Laulund, Lone W.; Lynch, Sally A.; Blyth, Moira; Prescott, Katrina; Canham, Natalie; Ibitoye, Rita; Brilstra, Eva H.; Shinawi, Marwan; Fassi, Emily; Sticht, Heinrich; Gregor, Anne; Van Esch, Hilde; Zweier, Christiane
Genet Med
Genetics in Medicine, 21, 12, pp. 2723-2733
Konrad, E D H, Nardini, N, Caliebe, A, Nagel, I, Young, D, Horvath, G, Santoro, S L, Shuss, C, Ziegler, A, Bonneau, D, Kempers, M, Pfundt, R, Legius, E, Bouman, A, Stuurman, K E, Õunap, K, Pajusalu, S, Wojcik, M H, Vasileiou, G, Le Guyader, G, Schnelle, H M, Berland, S, Zonneveld-Huijssoon, E, Kersten, S, Gupta, A, Blackburn, P R, Ellingson, M S, Ferber, M J, Dhamija, R, Klee, E W, McEntagart, M,Lichtenbelt , K D, Kenney, A, Vergano, S A, Abou Jamra, R, Platzer, K, Ella Pierpont, M, Khattar, D, Hopkin, R J, Martin, R J, Jongmans, M C J, Chang, V Y, Martinez-Agosto, J A, Kuismin, O, Kurki, M I, Pietiläinen, O, Palotie, A, Maarup, T J, Venborg Pedersen, K, Laulund, L W & DDD Study 2019, ' CTCF variants in 39 individuals with a variable neurodevelopmental disorder broaden the mutational and clinical spectrum ', Genetics in Medicine, vol. 21, no. 12, pp. 2723-2733 . https://doi.org/10.1038/s41436-019-0585-z
Genetics in Medicine, 21, 12, pp. 2723-2733
Konrad, E D H, Nardini, N, Caliebe, A, Nagel, I, Young, D, Horvath, G, Santoro, S L, Shuss, C, Ziegler, A, Bonneau, D, Kempers, M, Pfundt, R, Legius, E, Bouman, A, Stuurman, K E, Õunap, K, Pajusalu, S, Wojcik, M H, Vasileiou, G, Le Guyader, G, Schnelle, H M, Berland, S, Zonneveld-Huijssoon, E, Kersten, S, Gupta, A, Blackburn, P R, Ellingson, M S, Ferber, M J, Dhamija, R, Klee, E W, McEntagart, M,
Academic Journal
Fountain, Michael D. ; Oleson, David S. ; Rech, Megan E. ; Segebrecht, Lara ; Hunter, Jill V. ; McCarthy, John M. ; Lupo, Philip J. ; Holtgrewe, Manuel ; Moran, Rocio ; Rosenfeld, Jill A. ; Isidor, Bertrand ; Le Caignec, Cédric ; Saenz, Margarita S. ; Pedersen, Robert C. ; Morgan, Thomas M. ; Pfotenhauer, Jean P. ; Xia, Fan ; Bi, Weimin ; Kang, Sung-Hae L. ; Patel, Ankita ; Krantz, Ian D. ; Raible, Sarah E. ; Smith, Wendy ; Cristian, Ingrid ; Torti, Erin ; Juusola, Jane ; Millan, Francisca ; Wentzensen, Ingrid M. ; Person, Richard E. ; Küry, Sébastien ; Bézieau, Stéphane ; Uguen, Kévin ; Férec, Claude ; Munnich, Arnold ; van Haelst, Mieke ; Lichtenbelt, Klaske D. ; van Gassen, Koen ; Hagelstrom, Tanner ; Chawla, Aditi ; Perry, Denise L. ; Taft, Ryan J. ; Jones, Marilyn ; Masser-Frye, Diane ; Dyment, David ; Venkateswaran, Sunita ; Li, Chumei ; Escobar, Luis F. ; Horn, Denise ; Spillmann, Rebecca C. ; Peña, Loren ; Wierzba, Jolanta ; Strom, Tim M. ; Parenti, Ilaria ; Kaiser, Frank J. ; Ehmke, Nadja ; Schaaf, Christian P.
In Genetics in Medicine August 2019 21(8):1797-1807
Academic Journal
Villegas, Florian ; Lehalle, Daphné ; Mayer, Daniela ; Rittirsch, Melanie ; Stadler, Michael B. ; Zinner, Marietta ; Olivieri, Daniel ; Vabres, Pierre ; Duplomb-Jego, Laurence ; De Bont, Eveline S.J.M. ; Duffourd, Yannis ; Duijkers, Floor ; Avila, Magali ; Geneviève, David ; Houcinat, Nada ; Jouan, Thibaud ; Kuentz, Paul ; Lichtenbelt, Klaske D. ; Thauvin-Robinet, Christel ; St-Onge, Judith ; Thevenon, Julien ; van Gassen, Koen L.I. ; van Haelst, Mieke ; van Koningsbruggen, Silvana ; Hess, Daniel ; Smallwood, Sebastien A. ; Rivière, Jean-Baptiste ; Faivre, Laurence ; Betschinger, Joerg
In Cell Stem Cell 7 February 2019 24(2):257-270
Academic Journal
Nakashima, Mitsuko; Kato, Mitsuhiro; Matsukura, Masaru; Kira, Ryutaro; Ngu, Lock-Hock; Lichtenbelt, Klaske D.; van Gassen, Koen L. I.; Mitsuhashi, Satomi; Saitsu, Hirotomo; Matsumoto, Naomichi
Journal of Human Genetics. 65(9):727-734
Academic Journal
Van Opstal, Diane; van Maarle, Merel C; Lichtenbelt, Klaske; Weiss, Marjan M; Schuring-Blom, Heleen; Bhola, Shama L; Hoffer, Mariette J V; Huijsdens-van Amsterdam, Karin; Macville, Merryn V; Kooper, Angelique J A; Faas, Brigitte H W; Govaerts, Lutgarde; Tan-Sindhunata, Gita M; den Hollander, Nicolette; Feenstra, Ilse; Galjaard, Robert-Jan H; Oepkes, Dick; Ghesquiere, Stijn; Brouwer, Rutger W W; Beulen, Lean; Bollen, Sander; Elferink, Martin G; Straver, Roy; Henneman, Lidewij; Page-Christiaens, Godelieve C; Sistermans, Erik A
Genet Med
Van Opstal, D, van Maarle, M C,Lichtenbelt , K, Weiss, M M, Schuring-Blom, H, Bhola, S L, Hoffer, M J V, Huijsdens-van Amsterdam, K, Macville, M V, Kooper, A J A, Faas, B H W, Govaerts, L, Tan-Sindhunata, G M, den Hollander, N, Feenstra, I, Galjaard, R-J H, Oepkes, D, Ghesquiere, S, Brouwer, R W W, Beulen, L, Bollen, S, Elferink, M G, Straver, R, Henneman, L, Page-Christiaens, G C & Sistermans, E A 2018, 'Origin and clinical relevance of chromosomal aberrations other than the common trisomies detected by genome-wide NIPS : results of the TRIDENT study', Genetics in Medicine, vol. 20, no. 5, pp. 480-485. https://doi.org/10.1038/gim.2017.132, https://doi.org/10.1038/gim.2017.132
Genetics in Medicine, 20, 5, pp. 480-485
Van Opstal, D, van Maarle, M C,
Genetics in Medicine, 20, 5, pp. 480-485
Academic Journal
van Rijn, Jorik M. ; Ardy, Rico Chandra ; Kuloğlu, Zarife ; Härter, Bettina ; van Haaften-Visser, Désirée Y. ; van der Doef, Hubert P.J. ; van Hoesel, Marliek ; Kansu, Aydan ; van Vugt, Anke H.M. ; Thian, Marini ; Kokke, Freddy T.M. ; Krolo, Ana ; Başaran, Meryem Keçeli ; Kaya, Neslihan Gurcan ; Aksu, Aysel Ünlüsoy ; Dalgıç, Buket ; Ozcay, Figen ; Baris, Zeren ; Kain, Renate ; Stigter, Edwin C.A. ; Lichtenbelt, Klaske D. ; Massink, Maarten P.G. ; Duran, Karen J. ; Verheij, Joke B.G.M ; Lugtenberg, Dorien ; Nikkels, Peter G.J. ; Brouwer, Henricus G.F. ; Verkade, Henkjan J. ; Scheenstra, René ; Spee, Bart ; Nieuwenhuis, Edward E.S. ; Coffer, Paul J. ; Janecke, Andreas R. ; van Haaften, Gijs ; Houwen, Roderick H.J. ; Müller, Thomas ; Middendorp, Sabine ; Boztug, Kaan
In Gastroenterology July 2018 155(1):130-143
Academic Journal
Bibiche den Hollander; Anne Rasing; Merel A. Post; Willemijn M. Klein; Machteld M. Oud; Marion M. Brands; Lonneke de Boer; Udo F. H. Engelke; Peter van Essen; Sabine A. Fuchs; Charlotte A. Haaxma; Brynjar O. Jensson; Leo A. J. Kluijtmans; Anna Lengyel; Klaske D. Lichtenbelt; Elsebet Østergaard; Gera Peters; Ramona Salvarinova; Marleen E. H. Simon; Kari Stefansson; Ólafur Thorarensen; Ulrike Ulmen; Karlien L. M. Coene; Michèl A. Willemsen; Dirk J. Lefeber; Clara D. M. van Karnebeek
Frontiers in Neurology, Vol 12 (2021)
Academic Journal
Glen R. Monroe; Albertien M. van Eerde; Federico Tessadori; Karen J. Duran; Sanne M. C. Savelberg; Johanna C. van Alfen; Paulien A. Terhal; Saskia N. van der Crabben; Klaske D. Lichtenbelt; Sabine A. Fuchs; Johan Gerrits; Markus J. van Roosmalen; Koen L. van Gassen; Mirjam van Aalderen; Bart G. Koot; Marlies Oostendorp; Marinus Duran; Gepke Visser; Tom J. de Koning; Francesco Calì; Paolo Bosco; Karin Geleijns; Monique G. M. de Sain-van der Velden; Nine V. Knoers; Jeroen Bakkers; Nanda M. Verhoeven-Duif; Gijs van Haaften; Judith J. Jans
Nature Communications, Vol 10, Iss 1, Pp 1-8 (2019)
Academic Journal
Houweling, Arjan C.; Beaman, Glenda M.; Postma, Alex V.; Gainous, T. Blair; Lichtenbelt, Klaske D.; Brancati, Francesco; Lopes, Filipa M.; van der Made, Ingeborg; Polstra, Abeltje M.; Robinson, Michael L.; Wright, Kevin D.; Ellingford, Jamie M.; Jackson, Ashley R.; Overwater, Eline; Genesio, Rita; Romano, Silvio; Camerota, Letizia; DAngelo, Emanuela; Meijers-Heijboer, Elizabeth J.; Christoffels, Vincent M.; McHugh, Kirk M.; Black, Brian L.; Newman, William G.; Woolf, Adrian S.; Creemers, Esther E.
Journal of Clinical Investigation. December, 2019, Vol. 129 Issue 12, p5374, 7 p.
Academic Journal
Ron Hochstenbach; Martin G. Elferink; Patrick H. A. vanZon; Klaske D. Lichtenbelt; Jeske vanHarssel; Heleen Schuring‐Blom; Godelieve C.M.L. Page‐Christiaens
Clinical Case Reports, Vol 6, Iss 5, Pp 788-791 (2018)
Academic Journal
Snoek, Rozemarijn; Albers, Marieke E.W.A.; Mulder, Eduard J.H.; Lichtenbelt, Klaske D.; de Vries, Linda S.; Nikkels, Peter G.J.; Cuppen, Inge; Pistorius, Lourens R.; Manten, Gwendolyn T.R.; de Heus, Roel
The Journal of Maternal-Fetal & Neonatal Medicine. 31:2188-2194
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