Answer:
Skeleton and the skeletal system
Explanation:
Answer:
DNA sequence from left to right
T G A G G A C T T
Explanation:
There are four DNA nitogenous base they include thymine, guanine, cytosine and Adenine. The Nitrogenous bases are complementary that is Adenine is complementary to thymine and cytosine is completely to quanine and they both can replace each other in this manner A-T,C-G and it means that Adenine can pair with thymine and cytosine can only pair with guanine. DNA is known as Deoxyribonucleic acid. DNA sequencing are shown usually from the 5' end to the 3' end . The sense strand in DNA is used in DNA sequences and also it has the antisense strand and also called the coding strand and the non-coding strand are information are contained in the sequence
What I know is that amino acid has side chain, amine groupe ,and groupe of carboxyl so what make them difference is side group where the is 20 different R-group which give each individual characteristics
Answer:
See the answer below
Explanation:
Let the disorder be represented by the allele a.
Since the disease is an autosomal recessive one, affected individuals will have the genotype aa and normal individuals will have the genotype Aa or AA.
Since the four adults are carriers, their genotypes would be Aa.
Aa x Aa
Progeny: AA 2Aa aa
Probability of being affected = 1/4
Probability of being a carrier = 1/2
Probability of not being affected = 3/4
(a) The chance that the child second child of Mary and Frank will have alkaptonuria = 1/2
(b) The chance that the third child of Sara and James will be free of the condition = 3/4
(c)
(d) If someone has no family history of the disorder, their genotype would be AA.
AA x aa
4 Aa
<em>The chance that a child with alkaptonuria will have an offspring with alkaptonuria if the child's mate has no family history </em>= 0
(e)
(f) <em>The chance that a child with alkaptonuria will have an offspring with alkaptonuria if the child's mate has no family history</em> = 0
