Homozygous α0 thalassemia (--/--) haplotype is associated with all the following, EXCEPT:
a) Homozygous deletion of beta genes
b) Deletion of all 4 alpha genes
c) Fetal death in-utero or soon after birth
d) Formation of hemoglobin tetramers such as β4 (Hemoglobin H)
e) Formation of hemoglobin tetramers such as γ4 (Hemoglobin Bart's)