A novel FY*A allele with the 265T and 298A SNPs formerly associated exclusively with the FY*B allele and weak Fyb antigen expression: implication for genotyping interpretative algorithms

By  

VOX SANGUINIS, Vol. 108, Iss. 1, 2015-01 ,pp. : 52-57

John Wiley & Sons Inc

Access to resources Recommend Favorite

A new ABCG2 null allele with a 27‐kb deletion including the promoter region causing the Jr(a−) phenotype

By  

TRANSFUSION, Vol. 55, Iss. 6pt2, 2015-06 ,pp. : 1467-1471

John Wiley & Sons Inc

Access to resources Recommend Favorite

Lewis histo‐blood group system phenotyping and genotyping reveal divergence in the association of Le(a−b−) phenotype and type 1 diabetes

By  

VOX SANGUINIS, Vol. 108, Iss. 3, 2015-04 ,pp. : 281-286

John Wiley & Sons Inc

Access to resources Recommend Favorite

Phenotype–genotype correlations in hemophilia A carriers are consistent with the binary role of the phase between F8 and X‐chromosome inactivation

By  

JOURNAL OF THROMBOSIS AND HAEMOSTASIS, Vol. 13, Iss. 4, 2015-04 ,pp. : 530-539

John Wiley & Sons Inc

Access to resources Recommend Favorite

High-resolution melting analysis using unlabeled probe and amplicon scanning simultaneously detects several lactase persistence variants

By Janukonyté Jurgita   Vestergaard Else M.   Ladefoged Søren A.   Nissen Peter H.  

Scandinavian Journal of Clinical and Laboratory Investigation, Vol. 70, Iss. 8, 2010-12 ,pp. : 535-540

Informa Healthcare

Access to resources Recommend Favorite