Authors: Ii, Setsuko Sobell, Janet L. Sommer, Steve S.

Citation: Ii, Setsuko et al., From molecular variant to disease: initial steps in evaluating the association of transthyretin M119 with disease., American journal of human genetics , 50-I(1), 1992, pp. 29-41

Authors: Koeberl, Dwight D. Bottema, Cynthia D. K Ketterling, Rhett P. Bridge, Peter J. Lillicrap, David P. Sommer, Steve S.

Citation: D. Koeberl, Dwight et al., Mutations causing hemophilia B: direct estimate of the underlying rates of spontaneous germ-line transitions, transversions, and deletions in a human gene., American journal of human genetics , 47-I(2), 1990, pp. 202-217

Authors: Koeberl, Dwight D. Bottema, Cynchia D. K. Buerstedde, Jean-Marie Sommer, Steve S.

Citation: D. Koeberl, Dwight et al., Functionally important regions of the factor 1X gene have a low rate of polymorphism and a high rate of mutation in the dinucleotide CpG, American journal of human genetics , 45-I(3), 1989, pp. 448-457

Authors: Bottema, Cynthia D. K. Ketterling, Rhett P. Ii, Setsuko Yoon, Hong-Sup Phillips, John A. Sommer, Steve S.

Citation: K. Bottema, Cynthia D. et al., Missense mutations and evolutionary conservation of amino acids: evidence that many of the amino acids in factor IX function as "spacer" elements., American journal of human genetics , 49-II(4), 1991, pp. 820-838

Authors: Bottema, Cynthia D. K. Ketterling, Rhett P. Yoon, Hong-Sup Sommer, Steve S.

Citation: K. Bottema, Cynthia D. et al., The pattern of factor IX germ-line mutation in Asians is similar to that of Caucasians., American journal of human genetics , 47-II(5), 1990, pp. 835-841