X chromosome.

Affected individuals have two copies of chromosome 18 plus extra material from chromosome 18 attached to another chromosome.

Chromosome 22 was the first human chromosome to be fully sequenced.

The chromosome with this allele became the Y chromosome, while the other member of the pair became the X chromosome.

Your mom could give this other X chromosome with that X chromosome.

So let's say that's an X chromosome and this is a Y chromosome.

Chromosome one, top left.

In humans, the SYCP1 gene is on chromosome 1p13 the SYCP2 gene is on chromosome 20q13.33 and the gene for SYCP3 is on chromosome 12q.

It's on the X chromosome.

Then you get a chromosome.

Artificially placing and expressing the Xist gene on another chromosome leads to silencing of that chromosome.

Because, after all, she inherits one chromosome from her mother, and one chromosome from her father.

The chromosome that was in the cell doesn't have one the chromosome we put in does.

The Z chromosome is larger and has more genes, like the X chromosome in the XY system.

Well, your mom could give this X chromosome, in conjunction with this X chromosome from your dad.

Chromosome constitution of races of maize.

The chromosome is literally blown apart.

So this is a single chromosome.

An inversion is a chromosome rearrangement in which a segment of a chromosome is reversed end to end.

Normally a chromosome has just one centromere, but in chromosome 2 there are remnants of a second centromere.

To compensate for the weight loss and to preserve metacentric height, the flight deck was covered with of concrete.

Chromosome 22 is the second smallest human chromosome (chromosome 21 being smaller), spanning about 49 million DNA base pairs and representing between 1.5 and 2 of the total DNA in cells.

Several genes have been associated with dyslexia, including DCDC2 and KIAA0319 on chromosome 6, and DYX1C1 on chromosome 15.

The new chromosome went into the cell.

The next level up is the chromosome.

And some of them have an X chromosome in them and some of them have a Y chromosome in them.

The chromosome number is 12, 24 or 36.

Now men, they only have one X chromosome.

And then the other one's a Y chromosome.

It is the result of a reciprocal translocation between chromosome 9 and chromosome 22, which is specifically designated t(9 22)(q34 q11).

If you get an x chromosome from your mom and an x chromosome from your dad, you're going to be a female.

In birds, the genes FET1 and ASW are found on the W chromosome for females, similar to how the Y chromosome contains SRY.

These are normally found only at the ends of a chromosome, but in chromosome 2 there are additional telomere sequences in the middle.

As a result, part of the BCR ( breakpoint cluster region ) gene from chromosome 22 is fused with the ABL gene on chromosome 9.

Virus chromosome relationships in cells of Rhynchosciara ( Diptera , Sciaridae ).

Chromosome 9 likely contains between 800 and 1,200 genes.

Chromosome 10 likely contains between 800 and 1,200 genes.

Chromosome 13 likely contains between 300 and 700 genes.

Chromosome 14 likely contains between 700 and 1,300 genes.

Chromosome 15 likely contains between 700 and 900 genes.

The WNT3 gene is located at human chromosome 17q21.

This huge package of DNA is called a chromosome.

Each tiny mass of DNA is called a chromosome.

So in this case, it'll be the Y chromosome.

So if you have an x chromosome and we'll talk about in a second why you can only get that from your mom an x chromosome from your mom and a y chromosome from your dad, you will be a male.