Awoman with color-normal vision, but whose father was color blind, marries a man with normal vision. they are expecting a child. they learn through genetic testing that their child will not be color blind. what is the probability that their child is a boy?

To know what happens here, you need to analyze the alleles.

If the father is color blind and the daughter is not, you can suppose that is a recessive allele.

You can tell she is a carrier only, and because we received one sexual allele from each parent. If they ask you about the gender, we can suppose a cross between Xx and XY being lower x the recessive allele (color-blind vision).

When you draw the Punnett square, you'll found the probabilities are XX, XY, Xx, and xY.

So, you have a 50% chance of having a boy and 25% chance of having a color-blind boy.

prophase: we can observe the chromosomes to coil up and condense. they become visible. nuclear membrane and envelope disintigrate.s

metaphase: chromosomes align at the center, the metaphase plate. spindle fibers attach to centromeres of the sister chromatids. they meet at kinetochores.

anaphase: sister chromatids are pulled towards each opposing centromere, set on different poles.

telophase: chromosomes are now clustered up only on either sides of the cell. nuclear membranes reform, and a new cell wall forms along the cell plate. this will lead to cytokinesis, the process that divides the cell membrane and forms the cell wall.

idk im sorry.