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chromosome translocation got it right from study island if that is what you are using it for. good luck on future questions

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Down syndrome is usually caused by an extra copy of what chromosome?

Down syndrome occurs because of the extra chromosome on chromosome 21. If you go onto google images and type in karyotype of Down syndrome, you will find a picture of the extra chromosome. Instead of having two chromosomes on chromosome 21, there is an extra. Type your answer here...


Why does wiskott aldrich syndrome only affect males?

I believe because it is linked to genetic x-chromosome sex-inherited trait, females have another x-chromosome whereas males do not


Is Down syndrome a single gene or polygenic trait?

Down syndrome is a result of having an extra chromosome in one's genes. Chromosome thirteen* if your that much into the science. It is also called trisomy 21 because the chromosome 21 is the one with the abnormalities. *Abnormalities with chromosome thirteen is called Patau syndrome or trisomy 13.


Turner's syndrome always results in female offsprings why?

Because people who have Turner syndrome have one X chromosome instead of the two other females have. As they do not have a Y chromosome, they are female.


What chromosome number is affected in Lowe syndrome?

Lowe syndrome is caused by a mutated gene on the X sex chromosome. Because it is X-linked, it occurs almost exclusively in males.


The type of Down syndrome that occurs because a section of chromosomes 21 attached to another chromosome is an example of a genetic disorder caused by?

chromosome translocation got it right from study island if that is what you are using it for. good luck on future questions


Why are women carriers of Lesch-Nyhan syndrome?

Females are considered to be carriers. This is because females have another X chromosome without the mutation that prevents them from getting this disease. If a woman is a carrier, she has a 50% risk to pass on her X chromosome with the mutation.


Which of the following are example(s) of trisomy---Turner Syndrome Down's Syndrome or Klinefelter's Syndrome?

Trisomy means having three copies of a chromosomes. Turner's syndrome is NOT an example of trisomy. Someone with Turner's syndrome has only one X chromosome. Down's syndrome IS an example of trisomy. Someone with Down's syndrome has 3 copies of chromosome 21. Klinefelter's syndrome is a tricky one. On one hand, it would be considered trisomy because they have 3 sex chromosomes. However, they are not all the SAME sex chromosomes. Someone with Klinefelter's has 2 X chromosomes and one Y chromosome.


What is nondisjunction and why is it harmful?

Nondisjunction is the failure of a homolog to separate during meiosis causing trisomy (an extra chromosome) or monosomy (a missing chromosome), it can be harmful because it is a mutation that can cause many devastating disease, for example nondisjunction of the 21st chromosome causes down syndrome, another example of nondisjunction being harmful, is nondisjunction of the sex chromosomes, causing Turner's or Klinefelter's syndrome two very devastating diseases.


What effect does Down syndrome have on the chromosomes?

Down syndrome is usually caused by a condition known as Trisomy 21, which means that a person has three copies of Chromosome 21, rather than the usual two copies. An extra chromosome is added. The normal amount is 46, but people with Down syndrome have 47.Occasionally, the condition is a result of part of Chromosome 21 becoming fused to the end of another chromosome.More info on Chromosome 21While Chromosome 21 isn't the shortest chromosome, it is the one that contains the fewest genes (other than the Y chromosome). This is because genes on Chromosome 22 are more closely spaced, and thus the chromosome contains more genes, despite its smaller size.


What is another name for down syndrom?

Well Down Syndrome is sometimes called Up Syndrome because most kids with Down Syndrome are very happy.Trisomy 21


Which syndrome is characterized by the XO chromosome abnormality?

Turner syndrome is characterized by an XO chromosome abnormality, where individuals have only one X chromosome instead of the usual two. This condition can lead to various physical and developmental abnormalities, such as short stature, heart defects, and infertility. Treatment may involve hormone therapy and fertility treatment.