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In document Science Focus 4 Textbook (Page 140-143)

Medical laboratory technician

Medical laboratory technicians carry out routine laboratory tests and other procedures for use in the diagnosis and treatment of diseases and disorders of the human body.

Medical laboratory technicians can be involved in: • setting up equipment used in the laboratory and

maintaining it in a clean condition

• preparing and staining slides of micro-organisms for examination

• testing and analysing blood, tissue or other body samples to determine blood types and composition, and to identify diseases

• analysing DNA samples to screen for diseases • communicating the results of tests to the medical

officers who have requested them.

A good medical laboratory technician will be able to: • work as part of a team with doctors, scientists and

laboratory assistants

• work accurately and with minimal supervision • do repetitive work without losing concentration

• keep accurate records and communicate well with others • apply scientific method to problems.

Fig 4.2.11

A medical laboratory technician preparing DNA for analysis

Human inheritance

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Questions ]

Checkpoint

Simple human inheritance

1 List three human conditions inherited through a single

gene.

2 Two ‘normal’ parents produce a child with a recessive

genetic characteristic being expressed. Identify whether the parents have homozygous or heterozygous genotypes.

3 State the probability of a recessive characteristic being

expressed in the child of parents who are:

a both homozygous for that characteristic and are

themselves affected by it

b both heterozygous for that characteristic

Blood groups

4 Describe the type of inheritance involved when Rh

blood groupings are inherited.

5 Outline the type of inheritance for the ABO blood group

system.

6 List the alleles of the ABO system.

7 Identify the codominant ABO allele, and the recessive

allele of the ABO system.

Other types of human inheritance

8 State the number of gene pairs thought to influence

eye colour.

9 Distinguish between continuous and discontinuous

variation.

10 List the two influences on intelligence.

Studying human inheritance

11 Studying human inheritance is complex. Identify the

main method of gathering information.

12 Draw the symbols used in pedigrees for a female,

identical twin boys, non-identical twin girls, and parents.

Sex-linked inheritance

13 Modify the following statements to make them correct. a The X chromosome is responsible for female

characteristics only.

b Males have the genotype XX.

c The Y chromosome carries more genetic coding than

the X chromosome.

d Sex-linked diseases occur because the Y

chromosome has fewer genes than the X.

e Diseases like haemophilia are inherited through males

in a family.

14 a Clarify what is meant by the term ‘a carrier’ of the

disease haemophilia.

b Explain whether a male can be a carrier of

haemophilia.

Think

15 Listed here are some characteristics:

height, ability to roll the tongue, skin colour, blood group

a From the list, identify two examples of characteristics

that show discontinuous variation within a population.

b From the list, identify two examples of characteristics

that show continuous variation within a population.

16 Cystic fibrosis is a disease carried by a single recessive

gene. Two unaffected parents have a child who suffers from the disease. Predict whether they will produce a child without the disease.

17 For each of the blood group genotypes listed below, identify the blood group phenotype.

a IA IA c IA IB e IB IO

b IA IO d IB IB f IO IO

18 An albino female and a non-albino male have two

children. One is non-albino, one is albino. Using the letters A for the dominant gene and a for the recessive gene, identify the genotypes of each of the children.

19 a If two albino people partner and produce a child, predict whether the child will be albino.

b If an albino person partners a person heterozygous

for albinism, predict the chances of their children being albino.

20 Explain why approximately half the human population

is female.

21 A genetic abnormality occurs where a person has the

genotype XXY. Would the person be male or female?

Justify your answer.

22 The ability to roll the tongue is a dominant characteristic.

Two people who cannot roll their tongue have four children. Predict how many of these children would be likely to be able to roll their tongue.

23 A child has blood group AB. The mother has blood

group A.

a Identify the possible blood group genotypes of the

father.

b Identify the possible blood groups of the father.

Analyse

24 ‘Sperm are either male or female’. Analyse this

statement, explaining whether the writer is correct, incorrect, or a bit of both, and justifying your answer.

>>>

26 Some people can roll their tongue into a U-shape.

Tongue rolling is controlled by a dominant gene (R) and a recessive gene (r). A pedigree for tongue rolling is shown in Figure 4.2.12. Identify the genotypes of each of these individuals.

a I male (generation I male) b II 1 c III 1 2 1 1 2 3 4 2 1 3 I II III IV Fig 4.2.12

Pedigree for tongue-rolling ability

Symbol Meaning

A Mating of a male and female

B Male with the inherited characteristic

C Identical twin boys

D Female without the inherited characteristic

E Deceased male

25 Identify the meaning that matches the pedigree symbol.

Skills

27 Construct a pedigree from the following information.

Jim and Jean are partners. They have four children: Scott, James, Natasha and Alan. James has a partner, Kylie.

[

Extension]

Investigate

1 a Gather information about the pedigree of a

champion horse or show dog.

b Construct a pedigree for your chosen animal. c Discuss the factors and outcomes that were

important when matings were chosen at each stage of the pedigree.

2 a Research the genetics of human blood groups,

and the problems raised by blood transfusions.

b Present a case study on one problem that has

occurred with a transfusion, explaining why the problem arose.

3 a Research some studies that have been conducted

concerning twins.

b Evaluate the evidence, summarising whether

heredity or environment is the major factor responsible for patterns of inheritance.

They have two children: Susan and Alison. Susan has a partner, Paul. They have three children: Anne, Emma and Colin. James, Natasha, Susan and Anne are all albino.

28 A man with blood group B and a woman with blood

group A produce a child. Predict the possible blood groups of the child by constructing a Punnett square.

29 Colour blindness is an X-linked recessive condition.

The symbols used to show the relevant genes are

Xn for the recessive allele on the X chromosome and XN for the normal gene on the X chromosome.

a Identify the genotypes of a non-colour-blind female,

a colour-blind female, a non-colour-blind male and a colour-blind male.

b If a colour-blind female partners a non-colour-blind

male, predict the chances of:

i their daughters being colour blind ii their sons being colour blind

30 Haemophilia is an X-linked recessive disease.

A heterozygous female does not show the disease. Her genotype is XHXh.

a Identify the genotype of: i a haemophiliac male

ii a non-haemophiliac male

b If the heterozygous female partners a non-

haemophiliac male, predict whether their sons will be haemophiliacs.

Human inheritance

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In document Science Focus 4 Textbook (Page 140-143)