And what’s the question?????
Answer:
(g o f)(x) = 
(not simplified)
Step-by-step explanation:
(g o f)(x) = g(f(x))
g(x) = 
f(x) = 
g(f(-5)) = g(
= 
= 
g(-170) = 
=
Answer:
The correct answer is - 1/2 or 50% for first and second child to be affected.
Step-by-step explanation:
Achondroplasia is an autosomal dominant disorder. Autosomal dominant disorder refers to the presence of a single copy of the defective gene that is enough to lead to dwarfness.
A cross of achondroplasia (Aa) parent to a person of normal height (aa) result in half of their children will be affected with dwarfism and the other half will be normal.
a cross between affected or dwarf and normal parent
Aa X aa
Punnett square:
a a
A Aa Aa
a aa aa
Aa- dwarfness
aa- normal height
The probability that both their first child and second child would have achondroplasia is
2/4 =1/2 or 50%.
Answer: B. 33.1
Step-by-step explanation:
Use sin to solve (opposite/hypotenuse)
let x= length of CV
sin(37)=x/55
x=55sin(37)
x≈33.1
5 2/5 would be converted to 5 6/15. you would then subtract the numerators and the whole numbers, giving you 3 5/15, which simplifies to 3 1/5
