The X can possibly be the sex chromosome. Like for human female we have the XX chromosomes and when the allele is on the X chromosome we write as X with a R as the superscript on top right.
Answer:
cardiovascular and respiratory systems
Explanation:
the cardiovascular system includes your heart and blood vessels, which function to remove deoxygenated blood from and return oxygenated blood throughout your body
Why are the seminal vesicles important for human reproduction?
This might help:
The seminal vesicles (Latin: glandulae vesiculosae), vesicular glands, or seminal glands, are a pair of simple tubular glands posteroinferior to the urinary bladder of some male mammals. Seminal vesicles are located within the pelvis. They secrete fluid that partly composes the semen.
They pass through the prostate, and open into the urethra at the seminal colliculus. During ejaculation, semen passes through the prostate gland, enters the urethra and exits the body via the urinary meatus.
I believe that the answer is:
A.
They allow the sperm to travel to the urethra to be released.
<h2>Down Syndrome</h2>
Explanation:
Down syndrome is a genetic disorder caused when abnormal cell division results in an extra full or partial copy of chromosome 21
- Down syndrome is a genetic disorder caused when abnormal cell division results in an extra full or partial copy of chromosome 21
- Down syndrome is usually caused by an error in cell division called nondisjunction which results in an embryo with three copies of chromosome 21 instead of the usual two
- Prior to or at conception, a pair of 21st chromosomes in either the sperm or the egg fails to separates
- With development in embryo the extra chromosome is replicated in every cell of the body;this type of Down syndrome which accounts for 95% of cases is called trisomy 21
- Maternal age is the only factor that has been linked to an increased chance of having a baby with Down syndrome resulting from nondisjunction;here environmental agents such as drugs, chemicals, and radiation act as mutagens which induce mutation in the fetus
