Is it a duplication of both the explicit plus family and the brittle XFMR1?

His words are unimportant and do not repeat them.

Sometimes it's true that a lot of things are repeated, and they are repeated twice.

I'm glad to answer your questions, it's not a repetition here, because the graphics card here is still very good, and its power is very low.

This is just its system settings, you don't need to repeat the settings, just set up the functions you set up at the beginning.

The real fun is that after you are knowledgeable, detached, and have a solid self-confidence, it is revealed in the verbal communication. Instead of putting on a show.

In this case, he is not repeating, in this case, because although their functions overlap to a certain extent, they still have their own roles relatively speaking.

These two must be repeated, so they cannot be used at the same time.

The Maixian Plus family and the Emerald Interstellar FMR 1 are both done, is it a duplicate? I think explicit plus thinning and brittleness do both repetitive.

If he does all of them, this and this are not duplicates, because they have certain subtle differences, mainly in their mode of operation.

Outside line plus+ information and brittleness, is this done repeatedly, isn't it different?

He's this thing, no, it's not repeated, he's the explicit and the emerald star, isn't he just cast in the same thing?

Nephew plus+ information and Cui Yixing plug FM re are not repeated, it is best to choose a repeat after the card.

Is the action of the outer string plus family and brittleness repeated, is it a repetition, and the two cannot be done at the same time?

Outside the risk plus drama and brittleness are done, is it to reorganize the two of them have their own functions? It's not cleverness, it's not repetition.

There are still a lot of tax increases for outsiders who don't, so you can check the content on the Internet.

Yes, if you do it all, there will be repetition, it will look like this.

The outer line is aerated and brittle, not repeated, not repeated.

This is indeed what it looks like, it's what you say, that's right, that's it, it's exactly the same as what you said.

One X chromosome CGG is repeated more than 200 times. If your husband's FMR1 CGG repeats less than 45 to 50 wild-type repeats, then you have a 50% chance that you will have a boy who is definitely sick, a 50% chance that he will be a healthy person with a normal genotype, a 50% chance that he will be a carrier of the disease-causing gene, and a 50% chance that he will be a healthy person with a normal genotype. Abnormal FMR1 gene is also related to premature ovarian failure.

Gene decoding has been very painful, and Jiaxue gene is worth recommending.

It is said that Jiaxue Gene has an infertility gene decoding to answer this kind of problem.

(1) According to the fact that human fragile X syndrome is caused by the duplication of a specific CGG GCC sequence in the FMR1 gene, which only exists on the X chromosome, it can be inferred that the type of variant that causes fragile X syndrome is a genetic mutation Investigating the incidence of a genetic disease is to randomly survey the population, dividing the number of people who develop the disease by the total number of people surveyed, and then multiplying by 100% Therefore, the incidence of fragile X syndrome = the number of people with fragile X syndrome 100% of the number of people surveyed

2) mRNA and proteins are produced by genes through the process of transcription and translation (3) According to the number 3 and 4 with nail disease and 10 is normal, it means that the mode of inheritance of nail disease is autosomal dominant 3 and 4 are both heterozygous, so the chance of having another child with nail disease is 3

4, the normal chance is 14

Since the female mated to number 7 does not contain the pre-mutated gene and the fully mutated gene, the chance of her offspring developing fragile X syndrome is 1 in 4 and is female

13 The chance of having both nail disease and fragile X syndrome is (1-23 12) 12 1

Therefore, the answers are: 1) Gene mutations Number of people with fragile X syndrome 100% (2) Transcription and translation.

3) Autosomal dominant inheritance 3

4 25% female.

The doctor gave me the exact same list as yours. I am Changping District Hospital. 3950.I'm still thinking about whether to do it at the district hospital, maybe somewhere else will save a little.

Have you done this check-up? This is also the list that was given to me