5.6

It runs in the family
5.6 The difference of being a boy or girl
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Slide 1: Slide
BiologieMiddelbare schoolhavo, vwoLeerjaar 2,3

This lesson contains 24 slides, with interactive quizzes, text slides and 1 video.

Items in this lesson

It runs in the family
5.6 The difference of being a boy or girl

Slide 1 - Slide

Let's repeat 5.5 first!

Slide 2 - Slide

What is a mutation?

Slide 3 - Open question

True or false:
A mutation usually doesn't have an effect in the phenotype
A
True
B
False

Slide 4 - Quiz

Are mutations always negative?
A
yes
B
no

Slide 5 - Quiz

In what type of cells do mutations have the greatest effect on our body?
A
red blood cell
B
egg cell
C
brain cell
D
white blood cell

Slide 6 - Quiz

True or false:
cancer can be the result of a mutation
A
True
B
False

Slide 7 - Quiz

Goals
- Why do certain inherited diseases occur more often in boys than in girls?
- Given a certain combination of parents, how can you determine the genotypes and phenotypes of sex-linked inherited characteristics in the off spring?



Slide 8 - Slide

One X of two X's

Slide 9 - Slide

The y chromosome

Slide 10 - Slide

Slide 11 - Slide

Could you see all the numbers?
Yes
Nothing
Not all of them

Slide 12 - Poll

Do you remember?
A recessive allele has to occur twice (on each chromosome) in order to be expressed. If a recessive allele is accompanied by a dominant allele on the other chromosome, the dominant allele will be expressed instead.

Slide 13 - Slide

Slide 14 - Slide

Take colour-blindness for example. This characteristic is caused by a recessive allele on the X chromosome. A boy with this allele on his X chromosome is colour-blind. A girl needs not one, but two recessive alleles to be colour-blind.



Slide 15 - Slide

Color-blindness
XB stands for normal vision
Xb stands for colour-blindness
The mother is a carrier for colour-blindness: XB Xb
The father is not colour-blind: XB Y

Slide 16 - Slide

Slide 17 - Slide

Can boys be carriers too for color blindness? Explain why/why not?

Slide 18 - Open question

It runs in the family
The last royal Russian couple (who lived at the beginning of the 20th century) were Tsar Nicholas Romanov and Tsarina Alexandra, who was a carrier for haemophilia. Although their four daughters, Olga, Tatiana, Maria and Anastasia, did not have haemophilia (some of them may have been carriers), the only son and heir to the throne, little prince Alexei unfortunately did.

Slide 19 - Slide

Question
What are the chances that one of Alexei his sisters was a carrier of haemophilia? Would Tsar Nicholas and Tsarina Alexandra always produce sons with haemophilia? Why or why not?

Slide 20 - Slide

What are the chances that one of Alexei’s sisters was a carrier of haemophilia?
A
0%
B
25%
C
50%
D
100%

Slide 21 - Quiz

Would Tsar Nicholas and Tsarina Alexandra always produce sons with haemophilia?
A
Yes
B
No

Slide 22 - Quiz

Slide 23 - Video

5.6
make the assignment
check your answers

Slide 24 - Slide