B 9.2 Inheritance Flashcards

(15 cards)

1
Q

What is a chromosome?

A

A long strand of DNA found in the nucleus that contains many genes.

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2
Q

What is a gene?

A

A short section of DNA that codes for a specific protein.

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3
Q

What is an allele?

A

A different version of a gene.

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4
Q

What is the difference between dominant and recessive alleles?

A

Dominant alleles are always expressed if present; recessive alleles are only expressed if both copies are recessive.

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5
Q

What is meant by homozygous?

A

Having two identical alleles for a particular gene (e.g., BB or bb).

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6
Q

What is meant by heterozygous?

A

Having two different alleles for a particular gene (e.g., Bb).

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7
Q

What is a genotype?

A

The genetic makeup of an organism — the alleles it possesses.

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8
Q

What is a phenotype?

A

The observable characteristics of an organism.

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9
Q

What is a genetic cross?

A

A diagram used to show the possible combinations of alleles inherited from parents.

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10
Q

What are the chances of a child having a dominant trait if both parents are heterozygous (e.g., Bb x Bb)?

A

75% (3 in 4)

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11
Q

What is cystic fibrosis caused by?

A

A recessive allele — both copies must be faulty for the disorder to appear.

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12
Q

What is polydactyly caused by?

A

A dominant allele — only one copy is needed to inherit the condition.

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13
Q

What is a carrier?

A

A person who has one copy of a recessive allele for a genetic condition but does not show symptoms.

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14
Q

What are some ethical issues with embryo screening?

A

Concerns include cost, discrimination, and the potential for ‘designer babies.’

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15
Q

Why might embryo screening be considered useful?

A

It can identify embryos with genetic disorders, helping parents make informed choices.

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