(i) What are multiple alleles? How do they differ from simple dominant-recessive allele pairs?
(ii) Explain the concept of multiple alleles with the help of a human trait studied by you.
(iii) Mention all possible genotypes with their corresponding phenotypes of the human trait as explained by you.
(iv) Comment on the type of inheritance pattern involved in the example explained by you.
A child with blood group A has father with blood group B and the mother with blood group AB. Choose the option that gives the correct genotypes of father, mother, and the child:

The diagram below shows the sequence of amino acids in part of haemoglobin molecule.
[Diagram: haemoglobin chain Val, His, Leu, Thr, Pro, Glu, Glu; mRNA line; DNA line with triplets CAT, GTA, AAT, TGA, GGA, CTT (the T marked with *), CTC. Key: Val = valine, His = histidine, Leu = leucine, Thr = threonine, Pro = proline, Glu = glutamic acid]
(i) If the base T (marked with *) is substituted with A, in "CTT" of DNA strand how would it affect the haemoglobin chain ?
(ii) Name the condition and the effects associated with the above substitution.

(i) Differentiate between Mendelian and Chromosomal disorders.
(ii) Which disorder is known as "Inborn Error of Metabolism" ? Mention its cause and any one symptom. Name the harmful compounds formed.
A woman having genes for haemophilia on one X chromosome and a gene for colour blindness on another X chromosome marries a normal man. The progeny will show