From HuGE Literature Finder Database
This database contains published literature on genetic associations and other human genome epidemiology
- 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 - A New IL-2RG Gene Mutation in an X-linked SCID Identified through TREC/KREC Screening: a Case Report.
Iranian journal of allergy, asthma, and immunology 2015 Aug 14 (4): 457-61.
Nourizadeh Maryam, Borte Stephan, Fazlollahi MohammadReza, Hammarström Lennart, Pourpak Zah - Spectrum of mutations in a cohort of UK patients with ADA deficient SCID: Segregation of genotypes with specific ethnicities.
Clinical immunology (Orlando, Fla.) 2015 Aug 161 (2): 174-179.
Adams Stuart P, Wilson Melanie, Harb Elissar, Fairbanks Lynette, Xu-Bayford Jinhua, Brown Lucie, Kearney Laura, Madkaikar Manisha, Bobby Gaspar - Clinical Characteristics and Genetic Profiles of 44 Patients with Severe Combined Immunodeficiency (SCID): Report from Shanghai, China (2004-2011).
Journal of clinical immunology 2012 Dec .
Yao CM, Han XH, Zhang YD, Zhang H, Jin YY, Cao RM, Wang X, Liu QH, Zhao W, Chen TX - Neonatal screening for severe primary immunodeficiency diseases using high-throughput triplex real-time PCR.
Blood 2012 Mar 119 (11): 2552-5.
Borte Stephan, von Döbeln Ulrika, Fasth Anders, Wang Ning, Janzi Magdalena, Winiarski Jacek, Sack Ulrich, Pan-Hammarström Qiang, Borte Michael, Hammarström Lenna
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