Tay-Sachs disease is caused by a mutation in the HEXA gene located on chromosome 15. Tay-Sachs follows an autosomal recessive pattern of inheritance. With the help of the diagram, identify which of the offspring will be an unaffected carrier.

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Answer:

B and C

Explanation:

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The branch of science which deals with genes and inheritance is called genetics.

The question is complete.

Please provide the information to know the answer.

  • Image of a pedigree.
  • The crosses between the parents.

This is the information required to solve the question.

Hence, provide the information.

For more information, refer to the link:-

https://brainly.com/question/19200238

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