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Page 1
Kinase mutant Btk results in atypical X-linked agammaglobulinaemia phenotype.
Gaspar HB, Ferrando M, Caragol I, Hernandez M, Bertran JM, De Gracia X, Lester T, Kinnon C, Ashton E, Espanol T. Gaspar HB, et al. Among authors: lester t. Clin Exp Immunol. 2000 May;120(2):346-50. doi: 10.1046/j.1365-2249.2000.01230.x. Clin Exp Immunol. 2000. PMID: 10792386 Free PMC article.
Rapid protein-based assays for the diagnosis of T-B+ severe combined immunodeficiency.
Gilmour KC, Cranston T, Loughlin S, Gwyther J, Lester T, Espanol T, Hernandez M, Savoldi G, Davies EG, Abinun M, Kinnon C, Jones A, Gaspar HB. Gilmour KC, et al. Among authors: lester t. Br J Haematol. 2001 Mar;112(3):671-6. doi: 10.1046/j.1365-2141.2001.02578.x. Br J Haematol. 2001. PMID: 11260071 Free article.
Direct binding of IL-12 to human and murine B lymphocytes.
Vogel LA, Showe LC, Lester TL, McNutt RM, Van Cleave VH, Metzger DW. Vogel LA, et al. Among authors: lester tl. Int Immunol. 1996 Dec;8(12):1955-62. doi: 10.1093/intimm/8.12.1955. Int Immunol. 1996. PMID: 8982780
Diagnostic value of exome and whole genome sequencing in craniosynostosis.
Miller KA, Twigg SR, McGowan SJ, Phipps JM, Fenwick AL, Johnson D, Wall SA, Noons P, Rees KE, Tidey EA, Craft J, Taylor J, Taylor JC, Goos JA, Swagemakers SM, Mathijssen IM, van der Spek PJ, Lord H, Lester T, Abid N, Cilliers D, Hurst JA, Morton JE, Sweeney E, Weber A, Wilson LC, Wilkie AO. Miller KA, et al. Among authors: lester t. J Med Genet. 2017 Apr;54(4):260-268. doi: 10.1136/jmedgenet-2016-104215. Epub 2016 Nov 24. J Med Genet. 2017. PMID: 27884935 Free PMC article.
SMAD6 variants in craniosynostosis: genotype and phenotype evaluation.
Calpena E, Cuellar A, Bala K, Swagemakers SMA, Koelling N, McGowan SJ, Phipps JM, Balasubramanian M, Cunningham ML, Douzgou S, Lattanzi W, Morton JEV, Shears D, Weber A, Wilson LC, Lord H, Lester T, Johnson D, Wall SA, Twigg SRF, Mathijssen IMJ, Boardman-Pretty F; Genomics England Research Consortium; Boyadjiev SA, Wilkie AOM. Calpena E, et al. Among authors: lester t. Genet Med. 2020 Sep;22(9):1498-1506. doi: 10.1038/s41436-020-0817-2. Epub 2020 Jun 5. Genet Med. 2020. PMID: 32499606 Free PMC article.
129 results