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homozygous organism is one which possess same genes on their chromosome pair for instance C which represent colour blindness it will be present on both the x chromosomes of a female.
A carrier for hemophilia refers to a female that has the genetic mutation for the disorder on one of her two X chromosomes. This means that she can pass the mutation on (with a 50% chance) to her children.
The term is monosomy, in which one chromosome of a pair is missing. Turner's Syndrome is an example of monosomy, in which there is only one sex chromosome, which is the X chromosome. Humans with Turner's Syndrome are female, but sterile. The genotype of the sex chromosomes in Turner's Syndrome is XO, in which O represents a missing chromosome.
No, 29 chromosomes is not a normal number for a female. Typically, females have 46 chromosomes, consisting of two copies of 23 chromosomes.
Female humans, and most other female mammals have two X sex chromosomes.
This is because mutations occur in x chromosomes. The male, who has "xy" sex chromosomes, will have the mutation if it is present in the x chromosome. Females, there is a smaller chance because there are two "xx" chromosomes, which reduces the chance that the mutation will be present.
An X linked carrier is one who carries a mutation in a gene found on the X sex chromosome. A carrier of the trait doesn't display phenotypic symptoms of the disease or mutation but can transfer the mutation in that gene to their offspring (ex: the carrier of a premutation that when transferred to the offspring via the X chromosome will cause the full mutation associated with that gene). A person could be a homozygous carrier if for instance, she were female (two X chromosomes) and carried the premutation associated with the disease. Some diseases need both alleles of the gene to be mutated. If only one allele is mutated (heterozygote) that person may be a carrier for that mutation and can thus pass on that mutation to their children.
homozygous organism is one which possess same genes on their chromosome pair for instance C which represent colour blindness it will be present on both the x chromosomes of a female.
A carrier for hemophilia refers to a female that has the genetic mutation for the disorder on one of her two X chromosomes. This means that she can pass the mutation on (with a 50% chance) to her children.
The term is monosomy, in which one chromosome of a pair is missing. Turner's Syndrome is an example of monosomy, in which there is only one sex chromosome, which is the X chromosome. Humans with Turner's Syndrome are female, but sterile. The genotype of the sex chromosomes in Turner's Syndrome is XO, in which O represents a missing chromosome.
Four types of chromosomal mutations are Down syndrome (which is a mutation in which there are three copies of chromosome 21), Kinefelter Syndrome (which is a mutation in which a male has an extra X-chromosome), Turner Syndrome (which is a mutation in which a female is missing an X-chromosome), and Patau Syndrome (which is a mutation in which there are three copies of chromosome 13).
No, 29 chromosomes is not a normal number for a female. Typically, females have 46 chromosomes, consisting of two copies of 23 chromosomes.
When there joined with a male chromosomes and a female chromosomes
Female humans, and most other female mammals have two X sex chromosomes.
There are 50 chromosomes in both male and female pineapple pollen grain.
They are passed on by male or female chromosomes.
Two X sex chromosomes are in a female liver cell.