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Immunologic Research|January 1, 1993
Complement biosynthesis by mononuclear phagocytesA R McPhaden, K WhaleyJournal of Clinical & Laboratory Immunology|January 1, 1982
Modulation of C2 biosynthesis by antigen-antibody complexesA R McPhaden, K WhaleyHuman Heredity|January 1, 1992
Type II hereditary angio-oedema associated with two mutations in one allele of the C1-inhibitor gene around the reactive-site coding regionZ Siddique, A R McPhaden, K WhaleyHuman Heredity|March 1, 1995
Characterisation of nucleotide sequence variants and disease-specific mutations involving the 3' end of the C1-inhibitor gene in hereditary angio-oedemaZ Siddique, A R McPhaden, K WhaleyHuman Genetics|September 1, 1993
C1-inhibitor gene nucleotide insertion causes type II hereditary angio-oedemaZ Siddique, A R McPhaden, K WhaleyClinical Genetics|March 1, 1991
Restriction fragment length polymorphism analysis of the C1-inhibitor gene in hereditary C1-inhibitor deficiencyA R McPhaden, G D Birnie, K WhaleyHuman Heredity|January 1, 1992
A single base deletion from the C1-inhibitor gene causes type I hereditary angio-oedemaZ Siddique, A R McPhaden, D McCluskey, et al.Human Genetics|December 1, 1991
An RNA splice site mutation in the C1-inhibitor gene causes type I hereditary angio-oedemaZ Siddique, A R McPhaden, D F Lappin, et al.Human Heredity|May 1, 1993
A point mutation in the C1-inhibitor gene causes type I hereditary angiooedemaZ Siddique, A R McPhaden, J E Fothergill, et al.Human Genetics|April 1, 1990
Regional assignment of the human C1-inhibitor gene to 11q11-q13.1A Theriault, K Whaley, A R McPhaden, et al.Pageof 16