Answer:
C. Emotional and behavioral disorders
Explanation:
Emotional and behavioral disorders are often difficult to define, but it is defined as :
- An inability to learn that cannot be explained by intellectual, sensory, or health factors.
- An inability to build or maintain satisfactory interpersonal relationships with peers and teachers.
- Inappropriate types of behaviors or feelings under normal circumstances.
- A general pervasive mood of unhappiness or depression.
- A tendency to develop physical symptoms related to fears associated with personal or school problems.
Hence , according to the scenario mentioned in the question, answer is C. Emotional and behavioral disorders.
Answer:
C. A gene is a segment of a DNA strand
Explanation:
Just took test
Answer:
Explanation:
A woman who is a carrier for #1 hemophilia and a man that does not have the
condition have children. What is the probability that they will have a child
with the condition being studied? What is the gender of that child?
if the baby gets the Y chromosome from the father it will be a boy. If the boy gets his mother's X chromosome with the hemophilia gene he will have hemophilia. If he inherits his mother's other X chromosome, he will have normal blood clotting. If the baby gets the X chromosome from the father it will be a girl.
#4 A woman that is heterozygous for type A blood and a man that is heterozygous for type B blood have children. What are the possible blood types of their children?
One parent with A and another with B can produce a child with A, B, AB or O blood types.
#5 Two people are both unknowingly carriers for the cystic fibrosis gene. What is the probability that they will have children with cystic fibrosis?
If both parents are carriers there is a 1 in 4 (25 percent) chance that both will pass on the non-functioning gene, which would result in a pregnancy affected with cystic fibrosis.
#3 A woman that is heterozygous for Huntington's disease and a man that does not have the condition have children . What is the probability that their children inherit the Huntington's gene ?
Huntington's disease (HD) is what is called a dominant genetic disease. What this usually means is that a child only has a chance of getting a disease like this if a parent has it too. But parents without HD can have a child with HD. This is true of any dominant genetic disease
The two ways by which we can detect that gene editing have occurred in the bacteria are;
A) WESTERN BLOT; Here,the gene that is edited will not be able to synthesize the protein.With this,if we do western against the already edited protein,no band will eventually appear in the western blot,and this indicates/confers that the gene have been edited.
B) PCR FOLLOWED BY SEQUENCING; IN PCR,there is amplification of the region with the use of flanking end primers that is edited.
However,mean primers will actually be used in a way that one primer is upstream to site of editing and the other primer to the downstream.
From this stage,the PCR product that is amplified will be sent for sequencing,and this sequency result will further confirm if the gene has been edited or not edited.
Restriction enzyme can also be used if the place where the gene has been edited is known.
If actually the gene has been edited,the nucleotide sequence will get changed.Having to choose such enzyme that cut only one's wide type wild type DNA but not actually gene that is edited,the result will further be compared inorder to confirm whether the gene has been edited or not.
