Question: How can you use a karyotype to diagnose a disease? 1. Compare: Select Subject C from the SIMULATION pane. Identify each of subject C's chromosomes, and
place them on the KARYOTYPING pane. Once you have completed the karyotype, take a loi snapshot of
it. Paste the coi snapshot into a document. Label it "Subject C."
How does subject C's karyotype differ from a normal karyotype?

Me with these questions if you’re it sure don’t answer

Refer to the family pedigree shown here. in generation i, one parent is affected by the gene mutation and one parent isn't. in generation ii, all three children are affected by the gene mutation. what can you conclude about this gene mutation? a. all children born in future generations will be affected by this disorder. b. this gene mutation is a dominant disorder. c. this gene mutation is a recessive disorder. d. the generation i mother is a carrier of this gene mutation.

The most famous fossil called archaeopteryx is which of the following? a dinosaur a fern a fish a bird