Answer:
Transphobia is a big one of course, but if she's family oriented, not being able to have a pregnancy and children of her own are a huge hit to the self esteem. I've also heard that the scarring from surgeries and dysphoria can make it unbearable at some points.
Explanation:
I have several trans friends, so it's always nice to spread information about these things when I can :)
Ok so lemme help u.
Every A becomes T and every C becomes G vice versa.
If you’re doing MRNA
Then instead of T you write U
The extra X chromosome is received from mother.
<h3><u>Explanation</u>:</h3>
Klinefelter's syndrome is the condition of chromosomal aberration where the person has an extra X chromosome. This means the genotype of the person is 44+XXY and the total chromosome number is 47. This condition is achieved due to inappropriate meiotic division and one of the sperm or ovum has the an extra X chromosome.
Here both the parents are normal in terms of colour vision. So the father cannot have the gene of colour blindness because if it was present, then father would have been colour blind because he has only one X chromosome per cell. So its present in mother who is heterozygous in terms of colour blind gene. So the extra X chromosome also came from her which made the presence of two defective X chromosomes in the offspring and made it colour blind.
<span>DNA stands for deoxyribonucleic
acid. The deoxy- in the DNA is a short term for deoxyribose. The nucleic acid
molecule has three parts; sugar, phosphate and a base. The phosphate in the DNA
acts as a backbone of the molecule. It is also responsible for the DNA’s
‘double-helix’ structure. The base has four codes namely adenine, thymine,
cytosine and guanine. Adenine and thymine are bse pairs whereas cytosine and
guanine are base pairs. They are not to be interchanged. Resulting in one cause
mutation in the gene. </span>
<span>The female is born with about one million immature sex cells.</span>