______G1. Define gene, allele and genome. _______
______G2. Define genotype, phenotype, dominant
allele, recessive allele, codominant alleles, locus, homozygous, heterozygous, carrier
and test cross. _______
______G3. Determine the genotypes and phenotypes of the
offspring of a monohybrid cross using a Punnett grid (square). _______
______ G4. State that some genes have more than two alleles (multiple
alleles). _______
______ G5. Describe ABO blood groups as an example of codominance and
multiple alleles. _______
______ G6. Explain how the sex is determined in humans. _______
______ G7. State that some genes are present on the X chromosome and
absent from the shorter Y chromosome in humans.
______ G8. Define sex linkage. ______
______G9. Explain how scientists can use
crossover frequency to determine the position of alleles on a chromosome
_______.
______ G10. Describe the inheritance of colour blindness
and hemophilia as examples of sex linkage. _______
_____ G11. Explain that female carriers are heterozygous for X-linked
recessive alleles. _____
_____ G12. Deduce the genotypes and phenotypes of individuals in
pedigree charts. _______
______G13. Explain the consequence of a base
substitution mutation in relation to the processes of transcription and
translation, using the example of sickle-cell anemia. ________
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