Answer:
loam
i am not 100% sure but logically it's loam
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Answer:
Complete question:
We are trying to determine the possible modes of inheritance for some particular human disorder. We have a very small pedigree for this disorder. Assuming the pedigree is accurate, indicate which of the six modes of inheritance are consistent with this pedigree: Select one or more Y Linked Autosomal Recessive Autosomal Dominant X-Linked Dominant X-Linked Recessive We are trying to determine the possible modes of inheritance for some particular human disorder. We have a very small pedigree for this disorder, Assuming the pedigree is accurate, indicate which of the six modes of inheritance ere consistent with this pedigree Select one or more X-Linked Recessive Y Linked Autosomal Recessive X-Linked Dominant Autosomal Dominant.
Answer:
After the analysis of this pedigree, it is clears that the inheritance pattern is X linked because the offsprings are affected with parents genotgype
Explanation:
The inheritance is X linked dominant because of the presence of one dominant gene for the affected genotype in male.
The male individuals are affected. This is therefore not a recessive inheritance in later case, it is only when the two genes are present at the same time the affected genotype will be seen.
The answer is Vitamin C otherwise known as Ascorbic acid. It is naturally present in some foods, added to others and available in dietary supplement. Fruits and vegetables are the best sources of vitam C. Citrus fruits, tomatoes and tomato juice and potatoes are major contributors of vitamin C.
Answer:
2) CAG - TTC - ACG mutates to CAG - TTC - ACC - ACG
Explanation:
Insertions are mutations in which extra base pairs are inserted into a new place in the DNA. The number of base pairs inserted can range from one to thousands!
In option no. 1: We see that there is not addition of a single or more than one base, but the new base sequence is different from the original sequence at three places i.e: TTA - CAC - G
In option no. 2: The insertion of three bases ACC has been made exactly after TTC, the whole sequence and arrangement of bases remain same except this insertion.
In option no. 3: The first base of the sequence T is replaced with A, and all other sequence is same. This type of mutation is called substitution in which one base is replaced by other.
In option no. 4: The last base of the sequence C is deleted, and is not present in new sequence. This type of mutation is called deletion in which a base is removed from the sequence.
Conclusion: Therefore, the best option is 2, in which whole codon is inserted in the DNA base sequence.
