Bio-Pac 06 Flashcards

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1
Q

Genotype

A

The gene combination.

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2
Q

Phenotype

A

The way an organism looks and behaves. (Two organisms can look alike (phenotype), but have different gene combinations (genotype )

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3
Q

Allele

A

Mendel concluded that each organism has two factors for each of its traits. These factors are genes and are located on the chromosomes. Genes exist in alternative forms. We call these different gene forms alleles .

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4
Q

Probability

A

The likelihood that each will occur .

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5
Q

Heterozygous

A

An organism is heterozygous for a trait if its two alleles for the trait are different .

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6
Q

Homozygous

A

An organism is homozygous for a trait if its two alleles for the trait are the same .

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7
Q

First Generation

A

The first generation of offspring. If both parents are homozygous for different genes/alleles then the first generation will have different genes, genotypes, and phenotypes than their parents. It was as if the recessive allele never existed .

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8
Q

Second Generation

A

The second generation of offspring. If both parents are heterozygous then the second generation will have the gene that disappeared in the first generation reappear one-fourth of the time in the second generation .

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9
Q

Hybrid

A

Heterozygous for a gene pair

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10
Q

Autosome

A

The 22 two pairs of matching homologous chromosomes that are NOT involved in sex determination.

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11
Q

Sex Chromosome

A

The two chromosomes that determine the sex of an individual.

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12
Q

Carrier

A

A carrier is a heterozygous individual appears the same phenotypically as onethat is homozygous dominant.

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13
Q

Nondisjunction

A

The failure of homologous chromosomes to separate properly during meiosis.

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14
Q

Purebred

A

Bred from parents that are homozygous for ALL their gene pairs.

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15
Q

Karyotype

A

Chart of homologous chromosomes pair.

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16
Q

Mutation

A

Any mistake or change in the DNA sequence.

17
Q

Mutagen

A

An agent that causes genetic mutation.

18
Q

Albinism

A

The absence of pigmentation in the eyes, skin, and hair.

19
Q

Amniocentesis

A

A common prenatal procedure that allows genetic analysis of fetal cells is amniocentesis.

20
Q

Hybrid

A

Heterozygous for a gene pair

21
Q

Autosome

A

The 22 two pairs of matching homologous chromosomes that are NOT involved in sex determination.

22
Q

Sex Chromosome

A

The two chromosomes that determine the sex of an individual.

23
Q

Carrier

A

A carrier is a heterozygous individual appears the same phenotypically as onethat is homozygous dominant.

24
Q

Nondisjunction

A

The failure of homologous chromosomes to separate properly during meiosis.

25
Q

Purebred

A

Bred from parents that are homozygous for ALL their gene pairs.

26
Q

Karyotype

A

Chart of homologous chromosomes pair.

27
Q

Mutation

A

Any mistake or change in the DNA sequence.

28
Q

Mutagen

A

An agent that causes genetic mutation.

29
Q

Albinism

A

The absence of pigmentation in the eyes, skin, and hair.

30
Q

Amniocentesis

A

A common prenatal procedure that allows genetic analysis of fetal cells is amniocentesis.