2.4 Antenatal & Postnatal Screening

Froggy Jumps

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About this activity

Screening questions covering modes of inheritance

Created by

Erin

United Kingdom

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2.4 Antenatal & Postnatal Screening


Froggy Jumps 2.4 Antenatal & Postnatal ScreeningOnline version Screening questions covering modes of inheritance by Erin 1 Can skip a generation a Autosomal Dominant b Autosomal Recessive c Incomplete Dominance 2 If the trait does not appear in a branch of a family tree it disappears from the family entirely a Autosomal Dominant b Autosomal Recessive c Incomplete Dominance 3 Trait is expressed in every generation a Autosomal Dominant b Sex-linked c Incomplete Dominance 4 Three phenotypes a Autosomal Dominant b Sex-linked c Incomplete Dominance 5 Sufferers are homozygous recessive (eg. hh) a Autosomal Recessive b Sex-linked c Incomplete Dominance 6 Affected males cannot pass the trait onto their sons a Autosomal Recessive b Sex-linked c Incomplete Dominance 7 Sufferers are homozygous dominant or heterozygous a Autosomal Recessive b Autosomal Dominant c Incomplete Dominance 8 More males are affected than females a Sex linked b Autosomal Recessive c Incomplete Dominance 9 Sufferers of the fully expressed form must have two parents with the partly expressed form a Autosomal Dominant b Autosomal Recessive c Incomplete Dominance 10 Suffers of the condition MUST have an affected parent a Autosomal Dominant b Autosomal Recessive c Incomplete Dominance 11 The fully expressed form is more rare. The partly expressed form is more common. a Autosomal Dominant b Sex linked c Incomplete Dominance 12 Females are rarely affected but may be carriers. a Autosomal Dominant b Sex linked c Incomplete Dominance

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2.4 Antenatal & Postnatal Screening

Froggy Jumps

About this activity

Created by

Download the paper version to play

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Froggy Jumps

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Froggy Jumps

2.4 Antenatal & Postnatal ScreeningOnline version

by Erin

Can skip a generation

If the trait does not appear in a branch of a family tree it disappears from the family entirely

Trait is expressed in every generation

Three phenotypes

Sufferers are homozygous recessive (eg. hh)

Affected males cannot pass the trait onto their sons

Sufferers are homozygous dominant or heterozygous

More males are affected than females

Sufferers of the fully expressed form must have two parents with the partly expressed form

Suffers of the condition MUST have an affected parent

The fully expressed form is more rare. The partly expressed form is more common.

Females are rarely affected but may be carriers.