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Related Questions

What is the difference between Edward's syndrome and Patau's syndrome?

in Patau there is an extra chromosome in chromosome 13, in Edwars it the extra chromosome is in chromosome 18


What chromosome is affected by Lobstein Syndrome?

13


Which chromosomes are effected in trisomy 13?

Patau syndrome is the result of trisomy 13. Trisomy 13 is usually caused by having an extra chromosome in every cell in the body. Every cell in the human body should contain two chromosomes, one from each parent, however every one in sixteen thousand newborn has three chromosomes. The result of a third chromosome can mean physical disabilities. Most children die within a few days after birth. The disease is not inherited.


What is 007 die another day rated?

PG-13


What is the presence of three of a particular chromosome?

The presence of three copies of a particular chromosome is known as trisomy. This genetic condition can lead to developmental abnormalities, such as Down syndrome which is caused by trisomy of chromosome 21.


How do you see mutation in a karyotype?

You might see an extra chromosome or a missing chromosome. You might see a piece of a chromosome missing, or a piece added onto another chromosome.


What is another word for colored bodies?

Chromosome


Which chromosome number does muscular dystrophy affect?

8 and 13


What number of chromosomes are affected in tourette syndrome?

Either chromosome 13 or 7. Mostly 13


What are four types of chromosomal mutations?

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).


What sex chromosome is present in all humans?

There are two sex chromosomes: the X chromosome and the Y chromosome. During fertilization, the mother always gives an X chromosome and the father gives either another X chromosome or a Y chromosome. Therefore, all humans have at least one X chromosome.


4 chromosome mutations?

Deletion: Part of a chromosome is missing. Duplication: A segment of a chromosome is copied multiple times. Inversion: A segment of a chromosome is reversed in orientation. Translocation: Part of a chromosome breaks off and attaches to another chromosome.