Biology, asked by JishnuMB, 8 months ago

The inheritance of two genctic diseases namely
phenylketonuria and haemophilia are to be studied
in two different individuals. Both these studies
will involve the use of :-
(1) Autosomes
(2) Sex chromosomes
(3) Restriction endonuclease
(4) Pedigree analysis​

Answers

Answered by adityaparashar1
1

Answer:

Let the dominant allele be 'A' and let the recessive allele be 'a'.

(a) Member 4 could be Aa (carrier) or aa (unaffected).

Member 5 is aa (affected).

Member 6 could be Aa (carrier) or aa (unaffected).

(b) Member 14 is a carrier female which means the genotype is Aa. Member 15 is an unaffected male (AA). So, the probability that the first child is a haemophilic male is 1/4

Explanation:

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