Polydactyly in humans is due to:

  • A
    Autosomal dominant gene
  • B
    Autosomal recessive gene
  • C
    Sex-linked dominant gene
  • D
    Sex-linked recessive gene

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Select the correct match.

$A$ colour-blind man marries the daughter of a colour-blind person. Then in their progeny:

$A$ son of a colourblind father and a normal homozygous mother marries a daughter of a normal father and a heterozygous (carrier) mother. What will be the phenotype of their children?

Give differences: Mendelian disorders and Chromosomal disorders.

If both parents are carriers for thalassaemia,which is an autosomal recessive disorder,what are the chances of pregnancy resulting in an affected child?

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