A karyotype would be useful in detecting:
A. a point mutation.
B. congenital birth defects.
C. which allele is present on a specific chromosome.
D. a translocation of one arm of a chromosome.
Option A: A point mutation affects only a single neucleotide. It is detected generally by .PCR based amplication tests,DNA microarray technology etc.
Option B: Congenital birth defects screening can be done through amniocentesis, chronic villus sampling and ultrasound
Option C: An allele is located on specific positions on specific chromosomes and its alternative form of a gene. Allelle Specific Amplification tests (AS -PCR). helps to detect them.
Correct option is Option D: translocation occurs when a part of chromosome breaks and reattaches to another. This can be detected using Karyotyping test. Karyotype tests detects the characteristics of the chromosomes (like their number,size and shape)
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