Zobrazeno 1 - 10
of 128
pro vyhledávání: '"Van Allen, Margot I"'
Autor:
Jacquinet, Adeline, Brown, Lindsay, Sawkins, Jessica, Liu, Pengfei, Pugash, Denise, Van Allen, Margot I., Patel, Millan S.
Publikováno v:
In European Journal of Medical Genetics May 2018 61(5):257-261
Autor:
Adam, Shelin, du Souich, Christèle, Elliott, Alison M., Lehman, Anna, Mwenifumbo, Jill, Nelson, Tanya N., van Karnebeek, Clara, Friedman, Jan M., Boelman, Cyrus, Bolbocean, Corneliu, Buerki, Sarah E., Candido, Tara, Eydoux, Patrice, Evans, Daniel M., Gibson, William, Horvath, Gabriella, Huh, Linda, Sinclair, Graham, Tarling, Tamsin, Toyota, Eric B., Townsend, Katelin N., Van Allen, Margot I., Vercauteren, Suzanne, Thouta, Samrat, Mancini, Grazia M.S., Naidu, Sakkubai, van Slegtenhorst, Marjon, McWalter, Kirsty, Person, Richard, Salvarinova, Ramona, Guella, Ilaria, McKenzie, Marna B., Datta, Anita, Connolly, Mary B., Kalkhoran, Somayeh Mojard, Poburko, Damon, Farrer, Matthew J., Demos, Michelle, Desai, Sonal, Claydon, Thomas
Publikováno v:
In The American Journal of Human Genetics 6 July 2017 101(1):65-74
Autor:
Horvath, Gabriella A., Demos, Michelle, Shyr, Casper, Matthews, Allison, Zhang, Linhua, Race, Simone, Stockler-Ipsiroglu, Sylvia, Van Allen, Margot I., Mancarci, Ogan, Toker, Lilah, Pavlidis, Paul, Ross, Colin J., Wasserman, Wyeth W., Trump, Natalie, Heales, Simon, Pope, Simon, Helen Cross, J., van Karnebeek, Clara D.M.
Publikováno v:
In Molecular Genetics and Metabolism January 2016 117(1):42-48
Autor:
Talkowski, Michael E., Mullegama, Sureni V., Rosenfeld, Jill A., van Bon, Bregje W.M., Shen, Yiping, Repnikova, Elena A., Gastier-Foster, Julie, Thrush, Devon Lamb, Kathiresan, Sekar, Ruderfer, Douglas M., Chiang, Colby, Hanscom, Carrie, Ernst, Carl, Lindgren, Amelia M., Morton, Cynthia C., An, Yu, Astbury, Caroline, Brueton, Louise A., Lichtenbelt, Klaske D., Ades, Lesley C., Fichera, Marco, Romano, Corrado, Innis, Jeffrey W., Williams, Charles A., Bartholomew, Dennis, Van Allen, Margot I., Parikh, Aditi, Zhang, Lilei, Wu, Bai-Lin, Pyatt, Robert E., Schwartz, Stuart, Shaffer, Lisa G., de Vries, Bert B.A., Gusella, James F., Elsea, Sarah H.
Publikováno v:
In The American Journal of Human Genetics 2011 89(4):551-563
Autor:
Nabais Sá, Maria J., El Tekle, Geniver, de Brouwer, Arjan P.M., Sawyer, Sarah L., del Gaudio, Daniela, Parker, Michael J., Kanani, Farah, van den Boogaard, Marie-José H., van Gassen, Koen, Van Allen, Margot I., Wierenga, Klaas, Purcarin, Gabriela, Elias, Ellen Roy, Begtrup, Amber, Keller-Ramey, Jennifer, Bernasocchi, Tiziano, van de Wiel, Laurens, Gilissen, Christian, Venselaar, Hanka, Pfundt, Rolph, Vissers, Lisenka E.L.M., Theurillat, Jean-Philippe P., de Vries, Bert B.A.
Publikováno v:
In The American Journal of Human Genetics 5 March 2020 106(3):405-411
Autor:
Friedman, J.M., Baross, Ágnes, Delaney, Allen D., Ally, Adrian, Arbour, Laura, Asano, Jennifer, Bailey, Dione K., Barber, Sarah, Birch, Patricia, Brown-John, Mabel, Cao, Manqiu, Chan, Susanna, Charest, David L., Farnoud, Noushin, Fernandes, Nicole, Flibotte, Stephane, Go, Anne, Gibson, William T., Holt, Robert A., Jones, Steven J.M., Kennedy, Giulia C., Krzywinski, Martin, Langlois, Sylvie, Li, Haiyan I., McGillivray, Barbara C., Nayar, Tarun, Pugh, Trevor J., Rajcan-Separovic, Evica, Schein, Jacqueline E., Schnerch, Angelique, Siddiqui, Asim, Van Allen, Margot I., Wilson, Gary, Yong, Siu-Li, Zahir, Farah, Eydoux, Patrice, Marra, Marco A.
Publikováno v:
In The American Journal of Human Genetics 2006 79(3):500-513
Akademický článek
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Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Angius, Andrea, Uva, Paolo, Oppo, Manuela, Buers, Insa, Persico, Ivana, Onano, Stefano, Cuccuru, Gianmauro, Van Allen, Margot I., Hulait, Gurdip, Aubertin, Gudrun, Muntoni, Francesco, Fry, Andrew E., Annerén, Göran, Stattin, Eva-Lena, Palomares-Bralo, María, Santos-Simarro, Fernando, Cucca, Francesco, Crisponi, Giangiorgio, Rutsch, Frank, Crisponi, Laura
Crisponi/cold‐induced sweating syndrome (CS/CISS) is a rare autosomal recessive disorder characterized by a complex phenotype (hyperthermia and feeding difficulties in the neonatal period, followed by scoliosis and paradoxical sweating induced by c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=core_ac_uk__::c45e82cb740a1d635000272492655055
https://orca.cardiff.ac.uk/id/eprint/121236/1/Angius_et_al-2019-Clinical_Genetics.pdf
https://orca.cardiff.ac.uk/id/eprint/121236/1/Angius_et_al-2019-Clinical_Genetics.pdf
Autor:
Philipp, Tom *, Feichtinger, Wilfried, Van Allen, Margot I., Separovic, Evica, Reiner, Angelika, Kalousek, Dagmar K.
Publikováno v:
In Fertility and Sterility 2004 82(5):1337-1342