Primary immunodeficiency diseases: Genomic approaches delineate heterogeneous Mendelian disorders.
dc.contributor.author | Ehlayel, MS | |
dc.contributor.author | Karaca, E | |
dc.contributor.author | Artac, H | |
dc.contributor.author | Bayram, Y | |
dc.contributor.author | Atik, MM | |
dc.contributor.author | Eldomery, MK | |
dc.contributor.author | Jolles, S | |
dc.contributor.author | Flatø, B | |
dc.contributor.author | Bertuch, AA | |
dc.contributor.author | Hu, J | |
dc.contributor.author | Walkiewicz, M | |
dc.contributor.author | Yang, Y | |
dc.contributor.author | Eng, CM | |
dc.contributor.author | Boerwinkle, E | |
dc.contributor.author | Gibbs, RA | |
dc.contributor.author | Shearer, WT | |
dc.contributor.author | Lyle, R | |
dc.contributor.author | Orange, JS | |
dc.contributor.author | Lupski, JR | |
dc.contributor.author | Yesil, Gözde | |
dc.contributor.author | Stray-Pedersen, A | |
dc.contributor.author | Sorte, HS | |
dc.contributor.author | Samarakoon, P | |
dc.contributor.author | Gambin, T | |
dc.contributor.author | Chinn, IK | |
dc.contributor.author | Coban, Akdemir | |
dc.contributor.author | Erichsen, HC | |
dc.contributor.author | Gu, S | |
dc.contributor.author | Hanson, IC | |
dc.contributor.author | Zhang, VW | |
dc.contributor.author | Wong, LJ | |
dc.contributor.author | Forbes, LR | |
dc.contributor.author | Yuan, B | |
dc.contributor.author | Jhangiani, SN | |
dc.contributor.author | Muzny, DM | |
dc.contributor.author | Rødningen, OK | |
dc.contributor.author | Sheng, Y | |
dc.contributor.author | Nicholas, SK | |
dc.contributor.author | Noroski, LM | |
dc.contributor.author | Seeborg, FO | |
dc.contributor.author | Davis, CM | |
dc.contributor.author | Canter, DL | |
dc.contributor.author | Mace, EM | |
dc.contributor.author | Vece, TJ | |
dc.contributor.author | Allen, CE | |
dc.contributor.author | Abhyankar, HA | |
dc.contributor.author | Boone, PM | |
dc.contributor.author | Beck, CR | |
dc.contributor.author | Wiszniewski, W | |
dc.contributor.author | Fevang, B | |
dc.contributor.author | Aukrust, P | |
dc.contributor.author | Tjønnfjord, GE | |
dc.contributor.author | Gedde-Dahl, T | |
dc.contributor.author | Hjorth-Hansen, H | |
dc.contributor.author | Dybedal, I | |
dc.contributor.author | Nordøy, I | |
dc.contributor.author | Jørgensen, SF | |
dc.contributor.author | Abrahamsen, TG | |
dc.contributor.author | Øverland, T | |
dc.contributor.author | Bechensteen, AG | |
dc.contributor.author | Skogen, V | |
dc.contributor.author | Osnes, LTN | |
dc.contributor.author | Kulseth, MA | |
dc.contributor.author | Prescott, TE | |
dc.contributor.author | Rustad, CF | |
dc.contributor.author | Heimdal, KR | |
dc.contributor.author | Belmont, JW | |
dc.contributor.author | Rider, NL | |
dc.contributor.author | Chinen, J | |
dc.contributor.author | Cao, TN | |
dc.contributor.author | Smith, EA | |
dc.contributor.author | Caldirola, MS | |
dc.contributor.author | Bezrodnik, L | |
dc.contributor.author | Lugo, Reyes | |
dc.contributor.author | Espinosa, Rosales | |
dc.contributor.author | Guerrero-Cursaru, ND | |
dc.contributor.author | Pedroza, LA | |
dc.contributor.author | Poli, CM | |
dc.contributor.author | Franco, JL | |
dc.contributor.author | Trujillo, Vargas | |
dc.contributor.author | Aldave, Becerra | |
dc.contributor.author | Wright, N | |
dc.contributor.author | Issekutz, TB | |
dc.contributor.author | Issekutz, AC | |
dc.contributor.author | Abbott, J | |
dc.contributor.author | Caldwell, JW | |
dc.contributor.author | Bayer, DK | |
dc.contributor.author | Chan, AY | |
dc.contributor.author | Aiuti, A | |
dc.contributor.author | Cancrini, C | |
dc.contributor.author | Holmberg, E | |
dc.contributor.author | West, C | |
dc.contributor.author | Burstedt, M | |
dc.date.accessioned | 2021-03-04T17:22:59Z | |
dc.date.available | 2021-03-04T17:22:59Z | |
dc.identifier.citation | Stray-Pedersen A., Sorte H., Samarakoon P., Gambin T., Chinn I., Coban A., Erichsen H., Forbes L., Gu S., Yuan B., et al., "Primary immunodeficiency diseases: Genomic approaches delineate heterogeneous Mendelian disorders.", The Journal of allergy and clinical immunology, cilt.139, ss.232-245, 2017 | |
dc.identifier.issn | 0091-6749 | |
dc.identifier.other | av_85d8886c-4d6c-41ed-a53e-232103b19aae | |
dc.identifier.other | vv_1032021 | |
dc.identifier.uri | http://hdl.handle.net/20.500.12627/90987 | |
dc.identifier.uri | https://doi.org/10.1016/j.jaci.2016.05.042 | |
dc.language.iso | eng | |
dc.title | Primary immunodeficiency diseases: Genomic approaches delineate heterogeneous Mendelian disorders. | |
dc.type | Makale | |
dc.relation.journal | The Journal of allergy and clinical immunology | |
dc.contributor.department | , , | |
dc.identifier.volume | 139 | |
dc.identifier.startpage | 232 | |
dc.identifier.endpage | 245 | |
dc.contributor.firstauthorID | 1042871 |
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