0
What else can I help you with?
What is the diagnostic tool that reveals missing or extra chromosomes and some structural changes in an individual's chromosomes?
A karyotype analysis is the diagnostic tool that reveals missing or extra chromosomes, as well as some structural changes in an individual's chromosomes. This test involves arranging and visualizing the chromosomes from a cell sample to identify abnormalities.
What mutation causes either the inclusion of an extra chromosomes in offspring or the deletion of an entire chromosomes?
non-disjunction
What clues to the presence of certain genetic disorders can be seen in a karyotypes?
-Extra, missing or damaged chromosomes could show the presence of genetic disorders.
Identify several things that can be seen with a karyotype?
A karyotype is the number and visual appearance of the chromosomes in the cell nuclei of an organism or species. A karyotype indicates gender, and whether there are any chromosomal abnormalities.
The failure of replicated chromosomes to separate is called?
The failure of replicated chromosomes to separate is called nondisjunction. This can lead to an abnormal number of chromosomes in daughter cells during cell division, which can result in genetic disorders such as Down syndrome.
When a child is born with extra or missing chromosomes?
Mental Retardation.
What is the diagnostic tool that reveals missing or extra chromosomes and some structural changes in an individual's chromosomes?
A karyotype analysis is the diagnostic tool that reveals missing or extra chromosomes, as well as some structural changes in an individual's chromosomes. This test involves arranging and visualizing the chromosomes from a cell sample to identify abnormalities.
What mutation causes either the inclusion of an extra chromosomes in offspring or the deletion of an entire chromosomes?
non-disjunction
What chromosomes do you get an extra copy for in humans that results in Down syndrome?
Down Syndrome is caused by a triplication of the 21st chromosome.
What are three disorders caused by missing or extra chromosomes?
1) down's syndrome2) turner syndrome3) jacob's syndrome
What happens if a human has too many or too few chromosomes?
It depends on which chromosomes were present as to what the abnormality would be, if any. If they were missing one or had one extra there would be developmental abnormalities.
What causes a baby to come out deformed?
Mutations in their chromosomal DNA. Each parent gives chromosomes to the baby, and when they meet sometimes there are doubles of chromosomes, missing chromosomes, or mutated chromosomes which cause abnormalities in the DNA and overall the child.
What causes a person to inherit an extra chromosome or to be missing a chromosome?
An individual inherits an extra chromosome or is missing one due to errors during cell division, specifically during meiosis or mitosis. These errors can lead to nondisjunction, where chromosomes fail to separate properly, resulting in gametes with an abnormal number of chromosomes. If such a gamete contributes to fertilization, the resulting embryo may have conditions like Down syndrome (trisomy 21, an extra chromosome) or Turner syndrome (monosomy X, a missing chromosome). Genetic factors and environmental influences may also play a role in the likelihood of these chromosomal abnormalities.
A photo of the chromosomes in a dividing cell arranged by size is an?
Karyotype. A karyotype is a visual representation of an individual's chromosomes arranged by size, shape, and banding pattern. It can be used to detect genetic abnormalities, such as extra or missing chromosomes.
What chromosomal abnormality causes Turner syndrome?
If one of sex chromosomes is missing. Normal-XX Turner- XO
Which mutation causes either the inclusion of an extra chromosomes. in offspring or the deletion of an entire chromosome?
non-disjunction
What clues to the presence of certain genetic disorders can be seen in a karyotypes?
-Extra, missing or damaged chromosomes could show the presence of genetic disorders.
