Albinism is caused by a recessive gen "c". A normal man marries an albino woman. The first son happened to be albino. What are the possible phenotypes of the parents? What is the chance that their other kids will be albino?
Alright, since "c" is recessive and the woman is albino, then the woman must be "c c" right? And since the son is albino, he must be "c c" too. Hence the father must have at least one "c". But since he is normal, then the other allele must NOT be "c" too (otherwise he would be albino).
My question is, when writing the Mendel table, how do I express that allele of the father (the one that is not "c")?
$$\begin{bmatrix} & c & c\\ ? & ?c & ?c\\ c & cc & cc\end{bmatrix}$$
I marked it with $?$ because I'm not sure what to put there. My first thought was "well, it could be a capital C I guess..." - but that doesn't sound right to me. A capital C would mean there is a dominant albinism allele (but I am told that albinism is recessive only...)
I can see clearly that there is a 50-50 chance of having albino kids. I just don't know how to draw that inheritance table.