The question is not complete. You need more context than this. What chromosome is it? 21? 23? 5? it autosomal? cmon man i cant answer this
They have 22 chromosome pairs or 44 chromosome and 2 sex cell. Here's a picture:
What differentiates a male from a female based off the chromosomes that are present is that a male organism will have X and Y chromosomes whereas a female organism will have X and X chromosomes.
There are two chromosomes that determine the sex of the baby, X and Y. The women's ova are always chromosome X and the male sperm determines the sex of the baby, having the option of being either X or Y. If the sperm is and X then the sex will be female, and if it is a Y it will be a male. XX=girl, XY=boy.
No, W and Z were just chosen as the names to distinguish them from X and Y.
There are a few types of Turner syndrome. The most common two are: 1) Classic - The karyotype is 45X. The second X chromosome in missing from all cells. 2) Mosaic - The karotype is 45X/46XX. The second X chromosome is missing from some cells. 3) There are other types of Turner syndrome in which the second X is only partly missing or it is partly damaged.
The trisomy 21 in a karyotype would look like extra chromosome 21 I ^^
They have 22 chromosome pairs or 44 chromosome and 2 sex cell. Here's a picture:
A karyotype tells you if you have the normal ammont of chromosomes (46 for humans), it can also tell you if you have more or less and if this is the case what it is that you have. The most common syndrome would be Down Syndrome, or trisomy 21. Down Syndrome is also called trisomy 21 because if you look at a karyotype from someone that has this syndrome then they have three coppies of the 21st chromosome.
The question is not really clear. A karyotype is the overall complement of chromosomes isolated from a cell or organism (eukaryotic). When the karyotype of a normal healthy female is prepared for viewing by a cytogeneticist, there are 22 pairs of autosomal chromosomes present (ie two of chromosome 1, two of chromosome 2 etc...). There is one additional pair of sex chromosomes (two copies of X). A normal healthy human male also has 22 pairs of autosomes but the pair of sex chromosomes is not matched but instead there is one X chromosome and one Y chromosome (which is smaller than the X). So, if you look at a karyotype that has been laid out - if the two sex chromosomes are different sizes (X and Y) then the karyotype is from a male, if however they are the same size (X and X) then the karyotype is from a female.
No. The X chromosome with the mutation will look no different than any other X chromosome. In order to see the mutation you would have to actually examine the base pairs and sequences. A single reversal, translation, deletion, or mutation of any kind within the specific segment of code can result in hemophilia. This will not result in an overall change in appearance of the chromosome.
like speghetti like speghetti
a Karyotype
Hemophilia is a Sex-linked genetic disorder. It is found on the X chromosome of chromosome 23.A carrier for Hemophilia(represented by H(dominant) or h(recessive)) would look like this:XHXh(Female)*Males are not carriers for hemophilia-They are either affected or they're not*An affected person would look like this:XhXh(Female) XhY(Male)Someone who is neither a carrier nor affected would look like this:XHXH(Female) XHY(Male)
The chromosome's role is to tell the stem cells what to make and how to look like. For example, if you have brown eyes, and the genetic code is 01001, then that is what the chromosome tells the cell to look like and function like.
No. People with Klinefelter's syndrome have a normal Y chromosome and 2 normal X chromosomes.
What differentiates a male from a female based off the chromosomes that are present is that a male organism will have X and Y chromosomes whereas a female organism will have X and X chromosomes.
then you know what your looking at and for