In this type of cross, the F1 generation will produce a summary the following offsprings; 4 children all homozygous normal for both the traits, 4 diheterozygous individuals for both traits, 4 individuals normal for the sickle cell trait but heterozygous for thelasemia trait, and finally, 4 individuals normal for thelasemia but heterozygous for the sickle cell trait, hence more or less carriers for thalasemia trait. Since heterozygous individuals for both the traits show no clinical symptoms, all the F1 generation children are considered healthy for the diseases that are as a result of the two traits, hence the probability of healthy children in this family will be 12/16, that is 0.75.
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