Point mutations causing the McLeod phenotype von Russo, David C.W., Lee, Soohee, Reid, Marion E., Redman, Colvin M.

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Mutations that diminish expression of Kell surface protein and lead to the Kmod RBC phenotype von Lee, Soohee, Russo, David C.W., Reid, Marion E., Redman, Colvin M.

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Molecular Defects Underlying the Kell Null Phenotype von Lee, Soohee, Russo, David C.W., Reiner, Alexander P., Lee, Jeffrey H., Sy, Michael Y., Telen, Marilyn J., Judd, W. John, Simon, Philippe, Rodrigues, Maria J., Chabert, Teresa, Poole, Joyce, Jovanovic-Srzentic, Snezana, Levene, Cyril, Yahalom, Vered, Redman, Colvin M.

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Mutations that diminish expression of Kell surface protein and lead to the K mod RBC phenotype von Lee, Soohee, Russo, David C.W., Reid, Marion E., Redman, Colvin M.

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The mouse Kell blood group gene (Kel): cDNA sequence, genomic organization, expression, and enzymatic function von Lee, S, Russo, D C, Pu, J, Ho, M, Redman, C M

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