AP BIOLOGY

HEREDITY

SEX LINKAGE

Question [CLICK ON ANY CHOICE TO KNOW THE RIGHT ANSWER]
Which genetic abnormality can be identified through karyotyping?
A
point mutation
B
recessive allele
C
extra chromosomes
D
sex-linked allele
Explanation: 

Detailed explanation-1: -A karyotype test checks the chromosomes in your cells to: See whether you have a full set of 46 chromosomes. Having too many or too few chromosomes can cause serious problems with health, growth, and normal development, such as Down syndrome (extra chromosome 21) and Turner syndrome (missing X chromosome).

Detailed explanation-2: -Karyotypes can reveal changes in chromosome number associated with aneuploid conditions, such as trisomy 21 (Down syndrome). Careful analysis of karyotypes can also reveal more subtle structural changes, such as chromosomal deletions, duplications, translocations, or inversions.

Detailed explanation-3: -A trisomy is a chromosomal condition characterised by an additional chromosome. A person with a trisomy has 47 chromosomes instead of 46. Down syndrome, Edward syndrome and Patau syndrome are the most common forms of trisomy.

There is 1 question to complete.