… As regards a mechanism by which thalassaemia genes … genes and genotypes in populations
(rather than in families) … suggested 79 per cent Caucasian genes in the population. The …

… associated with homologous genes or a single gene. … The frequency of k (Ag) is over 98%
of whites and blacks, K Ag … for phenotypic description but rarely applied. According to Wiener…

… and in Hispanics compared with Whites. Affected individuals are at … lesions in the same
ApoE-null mice likely brought upon by … alleles on an isogenic background may help to identify the …

… DARC belongs to a family of chemokine receptors that lack a G-… of human evolution, the
DARC-null allele is present in as high as … may explain how thalassemia protects against malaria. …

… all kinds of issues about race, our biracial families, and both of us having struggled as first-…
principal way that researchers have organized rare allelic changes that affect some aspect of …

… , jaundice in newborns, and icteriswhites of the eyes. Such symptoms … genes. These two
pairs are the human alpha-like globin … or inactive β-thalassemia known as β0-thalassemia, the …

… The aim of this thesis was to establish the molecular mechanisms … , a null phenotype may
also be due to alleles expressing inactive … of two families.When it was discovered in 1982 some …

… alleles of the ABO system are codominant, whereas the null … The ABO blood group is the
first molecular polymorphism to … Additionally, there may be avoidance of donations from family …

Patients with sickle cell disease (SCD) receive regular blood transfusions, which can lead to
alloimmunisation due to exposure to different red blood cell (RBC) antigens. The spleen is …

… methodology, adding the detection of more HLA-genes such as DPB1, … of the null phenotype,
rare blood, available only in rare blood … in SCD and β-thalassemia, fostered by the current …