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Results:
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Results: 3
Prenatal RHD gene determination and dosage analysis by PCR: clinical evaluation
Authors:
Chan, FY Cowley, NM Wolter, L Stone, M Carmody, F Saul, A Hyland, CA
Citation:
Fy. Chan et al., Prenatal RHD gene determination and dosage analysis by PCR: clinical evaluation, PRENAT DIAG, 21(4), 2001, pp. 321-326
RHD gene mutations and the weak D phenotype: An Australian blood donor study
Authors:
Cowley, NM Saul, A Hyland, A
Citation:
Nm. Cowley et al., RHD gene mutations and the weak D phenotype: An Australian blood donor study, VOX SANGUIN, 79(4), 2000, pp. 251-252
A single point mutation at a splice site generates a silent RH50 gene in acomposite heterozygous Rh-null blood donor
Authors:
Cowley, NM Saul, A Cartron, JP Hyland, CA
Citation:
Nm. Cowley et al., A single point mutation at a splice site generates a silent RH50 gene in acomposite heterozygous Rh-null blood donor, VOX SANGUIN, 76(4), 1999, pp. 247-248
Risultati:
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