Chapter 14-Chromosomes & Human Genetics Flashcards

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0
Q

Linkage can be disrupted by what?

A

Crossing over

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1
Q

Linkage

A

Genes on the same chromosome transmitting together in inheritance

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2
Q

Crossing over

A

An exchange of parts of homologous chromosomes (prophase l)

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3
Q

Crossing over results in what?

A

Genetic Recombination

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4
Q

Linkage group

A

A large number of linked genes on a specific chromosome

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5
Q

Genetic recombination

A

Combination of alleles that were not present in the parental cell

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6
Q

Changes in chromosome structure can lead to what?

A

Genetic abnormalities or disorders

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7
Q

Wild-type

A

Most common form of alleles

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8
Q

Less common form of an allele?

A

Mutant Allele

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9
Q

How many autosomes do human somatic cells have?

A

Human somatic cells have 22 pairs

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10
Q

Sex chromosomes determine what?

A

An individuals sex

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11
Q

All humans have how many pairs of sex chromosomes?

A

1 pair

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12
Q

An absence of a Y chromosomes results in what?

A

The formation of ovaries

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13
Q

What governs the development of testes?

A

A gene on the Y chromosome

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14
Q

What did Thomas Hunt Morgan discover?

A

Each gene has a specific location on a chromosome

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15
Q

The probability that a crossover will disrupt a linkage between 2 genes at 2 different loci is directly proportional to what?

A

The distance that separates the 2 loci

16
Q

What is a Pedigree?

A

Chart of genetic connections

17
Q

Genetic abnormality

A

Traits that are not inherently life-threatening

18
Q

Genetic Disorder

A

Causes medical problems that may be severe

19
Q

Single genes on autosomes or sex chromosomes govern what?

A

More than 6,000 genetic abnormalities

20
Q

Polygenic

A

Human traits influenced by multiple genes.

21
Q

List the variations in single genes

A
  • Autosomal dominant
  • Autosomal recessive
  • X linked recessive
  • X linked dominant
22
Q

List the variations in a whole chromosome

A

-Changes in chromosome number & structure

23
Q

List the reasons mutations survive in populations.

A
  • Reintroduction by new mutations
  • Recessive alleles are masked in heterozygotes
  • Heterozygotes have an advantage in their environment
24
Q

Autosomal Dominant Inheritance

Draw Punnet Square of a heterozygous parent and homozygous parent

A

At least one parent has to have a dominant allele (A) in order to have a 50/50 chance of the child being affected

25
Q

Autosomal Recessive Inheritance

Draw a Punnet Square of 2 heterozygous parents

A

Depending if the parents are a carrier of a recessive allele (a), they have a 25% chance their child will be affected (aa)

26
Q

List the 4 categories of chromosome aberration

A
  • Deletion
  • Duplication
  • Inversion
  • Translocation
27
Q

Nondisjunction

A

Causes changes in chromosomes number

28
Q

Aneuploidy

A

One extra or one less chromosome

29
Q

Polyploidy

A

Three or more of each chromosome