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sergey [27]
3 years ago
14

PLEASE HELP 47 POINTS ASAP

Biology
2 answers:
Studentka2010 [4]3 years ago
7 0

Answer:

Would It be C

Explanation:

I am so sorry but my brother said that he did it and he said he got it right but i was not for sure so .....:(

Leto [7]3 years ago
4 0

Answer:

The animals don't know outside of that habit because that where they were born. If they were to be released they would die because they are not used to having to fend for themselves.

Explanation:

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List two examples of temporary change in human​
weeeeeb [17]

Answer:

Being emotional

Frustrations about changes in bodies

Explanation:

During growth stage, there are certain changes that occurs, these changes are either permanent or temporary. Temporary changes are seasonal and end with time as one is transitioning whereas permanent changes like deepening of voice in boys remains and growth of breasts in girls are permanent

3 0
3 years ago
Is the sentence simple, compound, or complex? After we have finished grocery shopping, would you like to go to the library? A. c
Gemiola [76]

Answer:

C. Complex

Explanation:

8 0
4 years ago
Is the Andromeda galaxy bigger than the Milky Way?
9966 [12]

yes because the andromeda is farthest away and bigger

5 0
4 years ago
A person who regularly eats a high-protein diet needs to make sure they _____.
Step2247 [10]

Answer:

I think its a

Explanation:

Adding water is also helping  the body get the rest of nutrions that it needs to function and you need to at least need to add a bit of water in your diet your body

8 0
3 years ago
Galactosemia is an inherited disorder in humans. A person with the disorder cannot digest the sugars in milk. The allele for nor
Misha Larkins [42]

Answer:

Explanation:

Galactosemia is an inherited metabolic disorder caused by changes,  or mutations, in both copies of an individual’s GALT gene. In the majority of cases,  children with galactosemia do not have parents with galactosemia. Mother and father separately are a silent carrier of the condition, which is expressed in the child (autosomal recessive inheritance).

Each individual has two copies of the GALT gene – one from father and one from mother. In case of any changes of these genes (mutations) that prevents the gene from working correctly. In order to inherit galactosemia, it is necessary for a child to have two GALT gene changes. In case of one GALT gene change there is no galactosemia.

Infants with galactosemia may be identified through newborn screening programs or by symptoms that present during the first few weeks of life. Untreated infants develop liver and kidney disease, cataracts in their eyes, and serious infections.

4 0
3 years ago
Read 2 more answers
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