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Primary immunodeficiency mutation databases.
Vihinen M, Arredondo-Vega FX, Casanova JL, Etzioni A, Giliani S, Hammarström L, Hershfield MS, Heyworth PG, Hsu AP, Lähdesmäki A, Lappalainen I, Notarangelo LD, Puck JM, Reith W, Roos D, Schumacher RF, Schwarz K, Vezzoni P, Villa A, Väliaho J, Smith CI. Vihinen M, et al. Among authors: hammarstrom l. Adv Genet. 2001;43:103-88. doi: 10.1016/s0065-2660(01)43005-7. Adv Genet. 2001. PMID: 11037300 Review.
Cellular basis of immunodeficiency.
Smith CI, Hammarström L. Smith CI, et al. Among authors: hammarstrom l. Ann Clin Res. 1987;19(4):220-9. Ann Clin Res. 1987. PMID: 3314648 Review. No abstract available.
Molecular basis for human immunodeficiencies.
Hammarström L, Gillner M, Smith CI. Hammarström L, et al. Curr Opin Immunol. 1993 Aug;5(4):579-84. doi: 10.1016/0952-7915(93)90041-p. Curr Opin Immunol. 1993. PMID: 7692881 Review.
DNA rearrangements in human B- and T-cell malignancies.
Smith CI, Hammarström L. Smith CI, et al. Among authors: hammarstrom l. Med Oncol Tumor Pharmacother. 1986;3(3-4):153-7. doi: 10.1007/BF02934991. Med Oncol Tumor Pharmacother. 1986. PMID: 3543528 Review.
Absence of xid mutation in X-linked agammaglobulinaemia.
Vorechovsky I, Zhou JN, Hammarström L, Smith CI, Thomas JD, Paul WE, Notarangelo LD, Bernatowska-Matuszkiewicz E. Vorechovsky I, et al. Among authors: hammarstrom l. Lancet. 1993 Aug 28;342(8870):552. doi: 10.1016/0140-6736(93)91676-d. Lancet. 1993. PMID: 8102684 No abstract available.
1,041 results