Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: Syndrome and TNFRSF13B[original query] |
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Gender, genotype, and phenotype differences in Smith-Magenis syndrome: a meta-analysis of 105 cases. Clinical genetics 2007 Jun 71 (6): 540-50. Edelman E A, Girirajan S, Finucane B, Patel P I, Lupski J R, Smith A C M, Elsea S |
Novel mutations in TACI (TNFRSF13B) causing common variable immunodeficiency. Journal of clinical immunology 2009 Nov 29 (6): 777-85. Mohammadi Javad, Liu Chonghai, Aghamohammadi Asghar, Bergbreiter Astrid, Du Likun, Lu Jiayi, Rezaei Nima, Amirzargar Ali Akbar, Moin Mostafa, Salzer Ulrich, Pan-Hammarström Qiang, Hammarström Lenna |
Genome-wide association study of serum albumin:globulin ratio in Korean populations.
Journal of human genetics 2013 Mar 58 (3): 174-7. Hong Kyung-Won, Jin Hyun-Seok, Song Daesub, Kwak Hye-Kyoung, Kim Sung Soo, Kim Yeonju |
TNF receptor superfamily member 13b (TNFRSF13B) hemizygosity reveals transmembrane activator and CAML interactor haploinsufficiency at later stages of B-cell development. The Journal of allergy and clinical immunology 2015 Jun . Romberg Neil, Virdee Manmeet, Chamberlain Nicolas, Oe Tyler, Schickel Jean-Nicolas, Perkins Tiffany, Cantaert Tineke, Rachid Rima, Rosengren Sally, Palazzo Regina, Geha Raif, Cunningham-Rundles Charlotte, Meffre Er |
Genetic testing of Behçet's disease using next-generation sequencing to identify monogenic mimics and HLA-B*51. Rheumatology (Oxford, England) 2023 11 . Alice Burleigh, Ebun Omoyinmi, Charalampia Papadopoulou, Eslam Al-Abadi, Ying Hong, Fiona Price-Kuehne, Elena Moraitis, Hannah Titheradge, Francesca Montesi, Diane Xu, Despina Eleftheriou, Paul Brog |
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