Chapter 9 Pt 1 Flashcards

1
Q

Genetically determined classes of human blood that are based on the presence or absence of carbohydrates A and B on the surface of red blood cells.

A

ABO blood group

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2
Q

A form of human dwarfism caused by a single dominant allele; the homozygous condition is lethal.

A

Achondroplasia

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3
Q

An alternative version of a gene.

A

Allele

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4
Q

A technique for diagnosing genetic defects while a fetus is in the uterus. A sample of amniotic fluid, obtained by a needle inserted into the amnion, is analyzed for telltale chemicals and defective fetal cells.

A

Amniocentesis

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5
Q

An individual who is heterozygous for a recessively inherited disorder and who therefore does not show symptoms of that disorder but who may pass on the recessive allele to offspring.

A

Carrier

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6
Q

A heritable feature that varies among individuals within a population, such as flower color in pea plants.

A

Character

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7
Q

A technique for diagnosing genetic defects while the fetus is in an early development stage within the uterus. A small sample of the fetal portion of the placenta is removed and analyzed.

A

Chorionic villus sampling (CVS)

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8
Q

A basic principle in biology stating that genes are located on chromosomes and that the behavior of chromosomes during meiosis accounts for inheritance patterns.

A

Chromosome theory of inheritance

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9
Q

Inheritance pattern in which a heterozygote expresses the distinct trait of both alleles

A

Codominant

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10
Q

A type of inheritance in which the phenotypes of the heterozygote and dominant homozygote are indistinguishable.

A

Complete dominance

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11
Q

A mating of two sexually reproducing individuals; often used to describe a genetics experiment involving a controlled mating.

A

Cross

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12
Q

The fusion of sperm and egg derived from two different individuals.

A

Cross-fertilization

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13
Q

A genetic disease that occurs in people with two copies of a certain recessive allele; characterized by an excessive secretion of mucus and vulnerability to infection; fatal if untreated.

A

Cystic fibrosis

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14
Q

An experimental mating of individuals differing at two genetic loci.

A

Dihybrid cross

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15
Q

The allele that determines the phenotype of a gene when the individual is heterozygous for that gene.

A

Dominant allele

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16
Q

A human genetic disease caused by a sex-linked recessive allele; characterized by progressive weakening and a loss of muscle tissue.

A

Duchenne muscular dystrophy

17
Q

The offspring of two parental (P generation) individuals. This stands for first filial.

A

F1 generation

18
Q

The offspring of the F1 generation. This stands for second filial

A

F2 generation

19
Q

The genetic makeup of an organism.

A

Genotype

20
Q

A human genetic disease caused by a sex-linked recessive allele; characterized by excessive bleeding following injury.

A

Hemophilia

21
Q

Having two different alleles for a given gene.

A

Heterozygous

22
Q

Having two identical alleles for a given gene

A

Homozygous

23
Q

A human genetic disease caused by a dominant allele; characterized by uncontrollable body movements and degeneration of the nervous system; usually fatal 10-20 years after the onset of symptoms.

A

Huntington’s disease

24
Q

The offspring of parents of two different species or of two different varieties of one species; the offspring of two parents that differ in one or more inherited traits; an individual that is heterozygous for one or more pairs of genes.

A

Hybrid