5.6

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

In deze les zitten 24 slides, met interactieve quizzen, tekstslides en 1 video.

Onderdelen in deze les

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

Slide 1 - Tekstslide

Let's repeat 5.5 first!

Slide 2 - Tekstslide

What is a mutation?

Slide 3 - Open vraag

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

Slide 4 - Quizvraag

Are mutations always negative?
A
yes
B
no

Slide 5 - Quizvraag

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 - Quizvraag

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

Slide 7 - Quizvraag

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 - Tekstslide

One X of two X's

Slide 9 - Tekstslide

The y chromosome

Slide 10 - Tekstslide

Slide 11 - Tekstslide

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 - Tekstslide

Slide 14 - Tekstslide

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 - Tekstslide

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 - Tekstslide

Slide 17 - Tekstslide

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

Slide 18 - Open vraag

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 - Tekstslide

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 - Tekstslide

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 - Quizvraag

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

Slide 22 - Quizvraag

Slide 23 - Video

5.6
make the assignment
check your answers

Slide 24 - Tekstslide