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Sliva [168]
3 years ago
6

Pls help meeeeee plsssssss

Biology
1 answer:
masya89 [10]3 years ago
7 0
The answer for this particular problem is b I believe
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Kelp me plz question is above
Korolek [52]

Answer:

top: response bias, middle: question-wording bias, bottom: under-coverage

Explanation:

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3 years ago
Plant and animal cells are complex and contain many structures.<br><br> a. True<br> b. False
Alex_Xolod [135]

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false ig because animal cell is not complex(i am not sure)

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3 years ago
How can humans help the water cycle
marishachu [46]

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A number of human activities can impact on the water cycle: damming rivers for hydroelectricity, using water for farming, deforestation and the burning of fossil fuels

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4 years ago
What does the exoskeleton use to<br> power its movements?
Verdich [7]

Answer:

A powered exoskeleton (also known as power armor, powered armor, powered suit, cybernetic suit, cybernetic armor, exosuit, hardsuit, or exoframe) is a wearable mobile machine that is powered by a system of electric motors, pneumatics, levers, hydraulics, or a combination of technologies that allow for limb movement with increased strength and endurance.

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4 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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