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N M Cowley

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Vox Sanguinis|January 13, 2001
RHD gene mutations and the weak D phenotype: an Australian blood donor studyN M Cowley, A Saul, C A Hyland
Vox Sanguinis|July 8, 1999
A single point mutation at a splice site generates a silent RH50 gene in a composite heterozygous RHnull blood donorN M Cowley, A Saul, J Cartron, et al.
Prenatal Diagnosis|April 5, 2001
Prenatal RHD gene determination and dosage analysis by PCR: clinical evaluationF Y Chan, N M Cowley, L Wolter, et al.
Pageof 1

Showing results (1-10 of 3) with videos related to

Sort By:
Pageof 1
Vox Sanguinis|January 13, 2001
RHD gene mutations and the weak D phenotype: an Australian blood donor studyN M Cowley, A Saul, C A Hyland
Vox Sanguinis|July 8, 1999
A single point mutation at a splice site generates a silent RH50 gene in a composite heterozygous RHnull blood donorN M Cowley, A Saul, J Cartron, et al.
Prenatal Diagnosis|April 5, 2001
Prenatal RHD gene determination and dosage analysis by PCR: clinical evaluationF Y Chan, N M Cowley, L Wolter, et al.
Pageof 1