Characterization of Jk(a+weak): a new blood group phenotype associated with an altered JK01 allele von Wester, Elisabet S., Storry, Jill R., Olsson, Martin L.

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Erythroid urea transporter deficiency due to novel JK(null) alleles von Wester, Elisabet S, Johnson, Susan T, Copeland, Tama, Malde, Ranjan, Lee, Edmond, Storry, Jill R, Olsson, Martin L

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Erythroid urea transporter deficiency due to novel JKnull alleles von Wester, Elisabet S., Johnson, Susan T., Copeland, Tama, Malde, Ranjan, Lee, Edmond, Storry, Jill R., Olsson, Martin L.

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Genetic basis of the K0 phenotype in the Swedish population von Wester, Elisabet S., Storry, Jill R., Schneider, Karin, Nilsson Sojka, Birgitta, Poole, Joyce, Olsson, Martin L.

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Erythroid urea transporter deficiency due to novel JK null alleles von Wester, Elisabet S., Johnson, Susan T., Copeland, Tama, Malde, Ranjan, Lee, Edmond, Storry, Jill R., Olsson, Martin L.

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Erythroid urea transporter deficiency due to novel JKnullalleles von WESTER, Elisabet S, JOHNSON, Susan T, COPELAND, Tama, MALDE, Ranjan, LEE, Edmond, STORRY, Jill R, OLSSON, Martin L

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Genetic basis of the K 0 phenotype in the Swedish population von Wester, Elisabet S., Storry, Jill R., Schneider, Karin, Nilsson Sojka, Birgitta, Poole, Joyce, Olsson, Martin L.

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IMMUNOHEMATOLOGY: Genetic basis of the K sub(0) phenotype in the Swedish population von Wester, Elisabet S, Storry, Jill R, Schneider, Karin, Nilsson Sojka, Birgitta, Poole, Joyce, Olsson, Martin L

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Genetic basis of the K(0) phenotype in the Swedish population von Wester, Elisabet S, Storry, Jill R, Schneider, Karin, Nilsson Sojka, Birgitta, Poole, Joyce, Olsson, Martin L

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National centralization of Hirschsprung’s disease in Sweden: a comparison of postoperative outcome von Söderström, Linnea, Graneli, Christina, Rossi, Daniel, Hagelsteen, Kristine, Gunnarsdottir, Anna, Oddsberg, Jenny, Svensson, Pär-Johan, Borg, Helena, Bräutigam, Matilda, Gustafson, Elisabet, Löf Granström, Anna, Stenström, Pernilla, Wester, Tomas

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KEL02 alleles with alterations in and around exon 8 in individuals with apparent KEL:1,−2 phenotypes von Wester, E. S., Steffensen, R., Ligthart, P. C., Vad, J., De Haas, M., Storry, J. R., Olsson, M. L.

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National centralization of Hirschsprung's disease in Sweden : a comparison of postoperative outcome von Soderstrom, Linnea, Graneli, Christina, Rossi, Daniel, Hagelsteen, Kristine, Gunnarsdottir, Anna, Oddsberg, Jenny, Svensson, Pär-Johan, Borg, Helena, Braeutigam, Matilda, Gustafson, Elisabet K, Granstroem, Anna Lof, Stenström, Pernilla, Wester, Tomas

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Characterisation of weak and null phenotypes in the KEL and JK blood group systems von Sjöberg Wester, Elisabet

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A New Phenotype In The Jk Blood Group System Associated With An Altered Jk1 Allele von Sjöberg Wester, Elisabet, Watz, E., Storry, J. R., Olsson, Martin L

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Molecular analysis of DNA from Danish blood donors revealed a novel allele with a mutation in exon 8 resulting in a very weak K phenotype von Steffensen, R, Sjöberg Wester, Elisabet, Vad, J., Nielsen, K R, Fjordside, A L, Storry, J R, Olsson, Martin L

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