A normal female karyotype would be described as 46 XX. A karotype shows the pairs of metaphase chromosomes of an individual cell and sorted according to size.
The male karyotype has 46 chromosomes the same as the female karyotype:23 chromosomes are inherited from your father.
It means they are female.
I believe the answer to your question is 23.
Achondroplasia is caused by a mutation in the FGFR3 gene and is not related to a specific karyotype. It is inherited in an autosomal dominant pattern, and individuals with achondroplasia typically have a normal karyotype (46 chromosomes in humans).
The normal monoploid (n) # of a female sex cell is 23 chromosomes
There are 46 chromosomes in a human Karyotype.
The male karyotype has 46 chromosomes the same as the female karyotype:23 chromosomes are inherited from your father.
A karyogram is a photograph of an individual's chromosomes arranged in a standard format, while a karyotype is the set of chromosomes found within the nucleus of a eukaryotic cell. In simpler terms, the karyogram is the visual representation of the karyotype.
A human karyotype is the number and appearance of chromosomes in the nucleus of a human cell. It is usually depicted as a systematized arrangement of chromosome pairs according to their size, shape, and banding pattern. A normal human karyotype includes 46 chromosomes, with 22 pairs of autosomes and one pair of sex chromosomes.
It means they are female.
I believe the answer to your question is 23.
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.
The karyotype of the asexual organism would not contain homologous chromosomes
Achondroplasia is caused by a mutation in the FGFR3 gene and is not related to a specific karyotype. It is inherited in an autosomal dominant pattern, and individuals with achondroplasia typically have a normal karyotype (46 chromosomes in humans).
The karyotype of an XO human would be deficient one X chromosome, compared to that of a normal female, and it would result in a female. Normal human females only use one X chromosome, whereby one is inactivated, which is why an XO human is viable. An XXY human would have one extra X chromosome as compared to that of a normal male, and it would result in a male. Again, an X chromosome is inactivated, which is why an XXY human is viable. XO is referred to as Turner Syndrome. XXY is referred to as Klinefelter Syndrome.
The normal monoploid (n) # of a female sex cell is 23 chromosomes
The karyotype of the asexual organism would not contain homologous chromosomes