00:01
To answer this question, let's talk about inheritance.
00:02
It says, in humans, there is a disease called a phenyl ketoneuria, that is pqau, which is caused by a excessive allele.
00:09
So let's suppose that in this case, the homozygous dominant and the heterocygous are going to be for a normal person, while the homozygum recessive is going to be for pqau.
00:20
Now, it says, people with this allele have a defective enzyme and cannot break down the amino acid phenylalanine.
00:26
This disease can result in mental retardation or death.
00:30
Also in humans there is a condition called galactose intolerance or galactosinia, which is also caused by a recessive a little.
00:37
And in this case, you're going to use that g.
00:38
So when you have the homozygous dominant or the heterozygos, you're going to have, you're going to be normal, practically.
00:45
But when you have the homozybolysis, you're going to have galatoemia.
00:52
Garagosimia, okay? now, it says, in both diseases normal dominates over recessive.
01:00
Well, we have already know that.
01:02
If two adults were heterocygoyal for both traits, it means if both are heterocygose for both genes, what are the chances of having a child that is completely normal? so when they give you the specific genotype or phenotype that they want you to get, you can spare making a type -harmia pannide square that takes longer.
01:22
And in this case, you can make two monohalbohabular square crossing this one with this one and this one with this one.
01:28
Okay, so you have the heterocygoyles e with the heterocylus e, you have small -saccharacteroid.
01:34
Heterocygote, heterocyg, homocybozygos, the same for the g, have the heterocyg with the heterocylus g you have homocygous g, homozygos, heterocygous, and homocygose, recessive.
01:48
So, in this case, they are asking you for the chances that they have a child that is completely normal...