By karyotype we will be able to detect the genetic abnormalities. Once the doctor have any doubt whether the patient have any genetic abnormality, they will suggest for karyotyping. By understanding the interpretation of karyotype doctors can easily counsel the patient and lead them in proper way...
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A karyotype can tell if the person contain a disease or illness because looking at the family line can tell the difference and can spot any disorders.
Doctors can use karyotypes to determine the sex of an individual. They can also use karyotypes to determine whether an individual has an abnormal number of chromosomes or noticeable chromosomal mutations, such as large deletions, additions, or translocations.
Cells in metaphase are used to produce karyotypes.
today doctors use tools such as amniocentesis and karyotypes to help detect genetic disorder.
there are no karyotypes of diabetes
karyotypes
Karyotypes, along with morphogens, determine the Physical Shape of Organisms.
by the single pair of sex chromosomes
Karyotyping is a diagram of ones chromosomes and is used to help determine if a baby will inherit any genetic disorders. Overall, Karyotyping is useful in studing chromosomes and how they work.
It can be used to know if a human (usually pre-born babies) has any chromosomal mutations and what is the person's sex.
Asymmetric karyotypes that are composed of small and large chromosomes with no intermediates states (bimodal karyotypes),for example Agave and Yucca genera from the family Agavaceae.
All of the chromosomes found in an organism.
A karyotype is the characteristic chromosome complement of a eukaryote species. In essence karyotypes describe your chromosomes. for more information go to http://en.wikipedia.org/wiki/Karyotype