Female transmit 23 chromosomes to the offspring. She has that unique chromosome called as X chromosome. This is transmitted to the offspring. From male you get either X or Y chromosome. From XX chromosome you get female child. From XY chromosome you get male child.
Do you mean as males's chromosome is sperm? I think it is egg cells for the females.
Why a female carried always an X chromosomes
Female transmit 23 chromosomes to the offspring. She has that unique chromosome called as X chromosome. This is transmitted to the offspring. From male you get either X or Y chromosome. From XX chromosome you get female child. From XY chromosome you get male child.
Males transmit one X chromosome and one Y chromosome to their offspring. There are very few genes carried on the Y chromosome.
The X chromosome belongs to both males and females. However, females have two of the same kind of sex chromosome(XX), and are called the homogametic sex. Males have two distinct sex chromosomes (XY), and are called the hetrogametic sex.
Chromosome map tells us about the deletion or insertion or a part of chromosome that is missed which may be a cause to any disorder.
the same type as any cell
Female transmit 23 chromosomes to the offspring. She has that unique chromosome called as X chromosome. This is transmitted to the offspring. From male you get either X or Y chromosome. From XX chromosome you get female child. From XY chromosome you get male child.
Males transmit one X chromosome and one Y chromosome to their offspring. There are very few genes carried on the Y chromosome.
recessive defect meaning that both copies of the chromosome must have the defect before it can be expressed. Females who have one X chromosome without the defect do not get this disease. Males, since they only have one X chromosome, get the disease
the frequencies with which the corresponding traits occur together in offspring.
The X chromosome belongs to both males and females. However, females have two of the same kind of sex chromosome(XX), and are called the homogametic sex. Males have two distinct sex chromosomes (XY), and are called the hetrogametic sex.
CGD is an X-linked genetic disease, meaning the defective gene is carried on the X chromosome (one of the sex chromosomes). Females have two copies of the X chromosome, whereas males have one X and one Y.
A chromosome is DNA in the nucleus of a cell.
The mutation must be present in the Reproductive cell, Ovum/Egg in females (present in the Ovary) and Sperm in males.
In one kind of abnormal chromosome inheritance called Down syndrome, a child has three copies of Chromosome 21!
well it depends on what kind of offspring
If the trait is recessive and on the male chromosome (Y), then it is impossible for females to get it since they do not possess a Y chromosome. If you meant a recessive sex-linked trait on the X chromosome (like male pattern baldness), then males are still more likely to get it since they only receive one X chromosome and if it is affected they would automatically have the trait (whereas females have 2 copies and would only have the trait if both parents passed on chromosomes containing the recessive allele.) Females can be carriers, though. If they are a carrier (have one affected X chromosome) for the trait then their male children would have a 50% chance of inheriting the trait and their female children would have a 50% chance of becoming carriers.
Grizzly bears offspring are called cubs.