Ask Question
26 March, 08:05

Suppose that a mother seeks genetic counseling because she is concerned that her child may have velocardiofacial syndrome, a syndrome that can result in symptoms such as a cleft palate and heart defects. The genetic counselor is aware that this disease is caused only by a small deletion in chromosome 22q11.2, that traditional karyotyping often overlooks. Consequently, the genetic counselor informs the mother that a cost-effective test will be conducted to visually detect the presence or absence of the specific chromosomal change by using velocardiofacial syndrome-specific probes and a sample of the child's DNA. To which technique is the genetic counselor likely referring?

O recombination frequency-based mapping

O fluorescence in situ hybridization (FISH)

O sequence tagged site (STS) mapping

O restriction fragment length polymorphism (RFLP) analysis

+2
Answers (1)
  1. 26 March, 08:08
    0
    Fluorescence in situ hybridization (FISH)

    Explanation:

    Fluorescence in situ hybridization (FISH) is a macromolecule acknowledgment innovation dependent on the correlative idea of DNA or DNA/RNA twofold strands. Chosen DNA strands joined with fluorophore-coupled nucleotides can be utilized as tests to hybridize onto the corresponding groupings in tried cells and tissues and afterward envisioned through a fluorescence magnifying instrument or an imaging framework. This innovation was at first evolved as a physical mapping apparatus to outline qualities inside chromosomes.
Know the Answer?
Not Sure About the Answer?
Find an answer to your question 👍 “Suppose that a mother seeks genetic counseling because she is concerned that her child may have velocardiofacial syndrome, a syndrome that ...” in 📗 Biology if the answers seem to be not correct or there’s no answer. Try a smart search to find answers to similar questions.
Search for Other Answers