• Korean Journal of Mathematics
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• v.31 no.1
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• pp.17-23
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• 2023

For a locus with two alleles (I^A and I^B), the frequencies of the alleles are represented by $$p=f(I^A)={\frac{2N_{AA}+N_{AB}}{2N}},\;q=f(I^B)={\frac{2N_{BB}+N_{AB}}{2N}}$$ where N_AA, N_AB and N_BB are the numbers of I^AI^A, I^AI^B and I^BI^B respectively and N is the total number of populations. The frequencies of the genotypes expected are calculated by using p², 2pq and q². Choi defined the density and operator for the value of the frequency of one gene and found the adapted partial differential equation as a follow-up for the frequency of alleles and applied this adapted partial differential equation to several diploid model [1]. In this paper, we find adapted equations for the model for selection against recessive homozygotes and in case that the alley frequency changes after one generation of selection when there is no dominance. Also we consider the triploid model with three alleles I^A, I^B and i and determine whether six genotypes observed are in Hardy-Weinburg for equilibrium.

• Journal of the Korean Mathematical Society
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• v.42 no.5
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• pp.1087-1100
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• 2005

In this note we give the mapping properties of the Marcinkiewicz integral !-to. at some end spaces. More precisely, we first prove that !-to. is a bounded operator from H$^{1,($\mathbb{R) to H$^{1, ($\mathbb{R). As a corollary of the results above, we obtain again the weak type (1,1) boundedness of $\mu$$_{, but the condition assumed on n is weaker than Stein's condition. Finally, we show that !-to. is bounded from BMO($\mathbb{R) to BMO($\mathbb{R). The results in this note are the extensions of the results obtained by Lee and Rim recently.