Análisis del seguimiento de pacientes Rh negativo en nuestro hospital: enero de 1983 a agosto 31 de 1984
Aguila Setién, Sonia; Noda García, Teresa.
Rev. cuba. obstet. ginecol
; 12(4): 421-30, oct.-dic. 1986. tab
Artículo en Español | CUMED | ID: cum-3551
Documentos relacionados
DEL variants: review of molecular mechanisms, clinical consequences and molecular testing strategy.
Patients with Asian-type DEL can safely be transfused with RhD-positive blood.
Overview of the serologic and molecular basis of D variants with a focus on D variants in the Indian population.
Molecular and serological analysis of the D variant in the Chinese population and identification of seven novel RHD alleles.
Transfusion support for a woman with <i>RHD*09.01.02</i> and the novel <i>RHD*01W.161</i> allele <i>in trans</i>.
RHD genotyping to resolve weak and discrepant RhD patient phenotypes.
RHD-negative red cells may be avoided for patients with ambiguous serologic typing for the RHD antigen.
Identification of <i>RHD</i> allelic variants discovered by atypical typing results on the NEO/Echo platforms.
Apparent changes in RhD status during pregnancy: A case study of weak D variant due to RHD*DAU-2.
Prediction of the antigenic regions in eight RhD variants identified by computational biology.