Answer:
es la c. trade winds o es la A. jet streams
Concentrate Odorants is the answer.
<span>After the third month of development, lanugo develops on the head (thin, first hair), the muscles and bones are formed an shaped, the mouth movement is possible, the liver and pancreas produce fluid secretions, meconium is made (stool of infant), reproductive organs are developed, but the baby's gender is difficult to distinguish on ultrasound.</span>
The pair of terms used to describe the location of the nose
when compared to the location of the eyes are medial and
inferior.
<h3>What is Location?</h3>
Location refers to the exact position of a particular object or
organism. In humans, location of different parts of the body
varies.
The location of the nose is medial to the eyes which means it is
found in the mid-line region of the eyes. The nose is also
inferior to the eyes as it is found in the lower region of where
the eye is located.
Read more about Location here brainly.com/question/1401793
The question is incomplete. The complete question is as follows:
Which of the following mutations is most likely to cause a phenotypic change?
A) a duplication of all or most introns
B) a large inversion whose ends are each in intergenic regions
C) a nucleotide substitution in an exon coding for a transmembrane domain
D) a single nucleotide deletion in an exon coding for an active site
E) a frameshift mutation one codon away from the 3' end of the nontemplate strand
Answer: D) a single nucleotide deletion in an exon coding for an active site
Explanation:
Deletion or insertion of a single nucleotide in an axon coding for an active site is called frameshift mutation.
The sequence of codons is read during translation, in order to synthesize a amino acids chain and form a protein from the nucleotide sequence. Frameshift mutations occur when the usual codon sequence is broken by the deletion or addition of one or more nucleotides. For example, if only one nucleotide is removed from the axon sequence during the RNA splicing process, then there will be a disrupted reading frame for all codons before and after the mutation. This may result in several incorrect amino acids being introduced into the protein. Disruption in protein sequence will cause phenotypic change.
Hence, the correct option is D) a single nucleotide deletion in an exon coding for an active site
.
