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Vanyuwa [196]
3 years ago
14

Do inner planets have a rocky surface

Biology
2 answers:
GREYUIT [131]3 years ago
6 0

Answer:

Yes

Explanation:

EastWind [94]3 years ago
4 0

Answer:

no

Explanation:

yes

sorry  it is a joke lol

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A pea plant that is homozygous for yellow pods with wrinkled seeds (ggrr) is cross-bred with a pea plant that is heterozygous fo
maria [59]
The correct genotypes of the parents are ggrr for yellow pods with wrinkled seeds and GgRr for <span>heterozygous for green pods with round seeds.
If the heterozygous individuals for both traits express have green pods and round seeds that tells us that these traits are dominant.
In the gross presented below, you can see that the offspring will have 4 different genotypes, all present in an equal percentage:
</span><span>gGrR 25% 
</span><span>gGrr  </span>25% 
<span>ggrR 25%
</span><span>ggrr 25%</span>

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3 years ago
Illnesses that pass from one organism to another are called _____ diseases.
Paraphin [41]
Sounds like infectious would fit. 
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3 years ago
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Tatiana [17]

In the citric acid cycle, the acetyl group of each molecule of acetyl-CoA is converted into two molecule of carbon dioxide and water. It is the pathway that connects carbohydrates ,fat and protein metabolism.

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Citric acid cycle is also known as krebs cycle or TCA cycle it is the series of chemical reactions to release to releases stored energy through the oxidation of acetyl-CoA from carbohydrate, fats and protein.

To learn more about Citric acid cycle here

brainly.com/question/11459709

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7 0
2 years ago
What is the condition in which the​ patient's pupils are normally​ unequal?
andrew11 [14]
The correct answer is "anisocoria". Anisocoria is the condition when the patient's pupils are normally unequal and the patient is asymptomatic and clinically stable. This should be differentiated in cases of patient with a relative afferent pupillary defect such is patients with optic neuritis or retinal detachment or in patients with neurological deficits.
3 0
3 years ago
NEED ANSWER
jolli1 [7]

Tay-Sachs disease is caused by mutations in the HEXA gene and inheritance is autosomal recessive . The HEXA gene gives the body instructions to make part of the beta-hexosaminidase A enzyme, which is needed to break down a substance called GM2 ganglioside.

i hope this helped! please mark me as brainliest and 5 stars >:)

7 0
3 years ago
Read 2 more answers
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