Knauth CM - Search Results

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Diverse and novel RHD variants in Australian blood donors with a weak D phenotype: implication for transfusion management.

McGowan EC, Lopez GH, Knauth CM, Liew YW, Condon JA, Ramadi L, Parsons K, Turner EM, Flower RL, Hyland CA. McGowan EC, et al. Among authors: knauth cm. Vox Sang. 2017 Apr;112(3):279-287. doi: 10.1111/vox.12488. Epub 2017 Feb 20. Vox Sang. 2017. PMID: 28220510

Investigation of the variable In(Lu) phenotype caused by KLF1 variants.

Fraser NS, Knauth CM, Schoeman EM, Moussa A, Perkins AC, Walsh T, Millard GM, Dean MM, Hyland CA, Flower RL. Fraser NS, et al. Among authors: knauth cm. Transfusion. 2018 Oct;58(10):2414-2420. doi: 10.1111/trf.14926. Epub 2018 Sep 17. Transfusion. 2018. PMID: 30222867

Genetic Variants Within the Erythroid Transcription Factor, KLF1, and Reduction of the Expression of Lutheran and Other Blood Group Antigens: Review of the In(Lu) Phenotype.

Fraser NS, Knauth CM, Moussa A, Dean MM, Hyland CA, Perkins AC, Flower RL, Schoeman EM. Fraser NS, et al. Among authors: knauth cm. Transfus Med Rev. 2019 Apr;33(2):111-117. doi: 10.1016/j.tmrv.2019.01.004. Epub 2019 Feb 7. Transfus Med Rev. 2019. PMID: 31023581 Review.

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