From HuGE Literature Finder Database
This database contains published literature on genetic associations and other human genome epidemiology
- Exome sequencing for simultaneous mutation screening in children with hemophagocytic lymphohistiocytosis.
International journal of hematology 2017 Mar .
Mukda Ekchol, Trachoo Objoon, Pasomsub Ekawat, Tiyasirichokchai Rawiphorn, Iemwimangsa Nareenart, Sosothikul Darintr, Chantratita Wasun, Pakakasama Sama - Common variants at PVT1, ATG13-AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency.
Nature genetics 2016 Nov 48 (11): 1425-1429.
Bronson Paola G, Chang Diana, Bhangale Tushar, Seldin Michael F, Ortmann Ward, Ferreira Ricardo C, Urcelay Elena, Pereira Luis Fernández, Martin Javier, Plebani Alessandro, Lougaris Vassilios, Friman Vanda, Freiberger Tomáš, Litzman Jiri, Thon Vojtech, Pan-Hammarström Qiang, Hammarström Lennart, Graham Robert R, Behrens Timothy - Targeted Sequencing and Immunological Analysis Reveal the Involvement of Primary Immunodeficiency Genes in Pediatric IBD: a Japanese Multicenter Study.
Journal of clinical immunology 2016 Oct .
Suzuki Tasuku, Sasahara Yoji, Kikuchi Atsuo, Kakuta Humihiko, Kashiwabara Toshihiko, Ishige Takashi, Nakayama Yoshiko, Tanaka Masanori, Hoshino Akihiro, Kanegane Hirokazu, Abukawa Daiki, Kure Shig - Eosinophilic gastroenteritis in a patient with Bruton's tyrosine kinase deficiency.
Pediatrics international : official journal of the Japan Pediatric Society 2016 Feb .
Yamazaki Susumu, Ohtsuka Yoshikazu, Yokokura Tomoaki, Yokota Rena, Honjo Asuka, Inage Eisuke, Baba Yosuke, Mori Mari, Suzuki Ryuyo, Iwata Tsutomu, Shimizu Toshia - Genotyping an immunodeficiency causing c.1624-11G>A ZAP70 mutation in Canadian Mennonites.
BMC medical genetics 2016 17 (1): 50.
Schroeder M L, Triggs-Raine B, Zelinski
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