Randomized Flashcards

1
Q

What is heredity?

A

Heredity is the passing on of traits from parents to their offspring; either through asexual reproduction or sexual reproduction.

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2
Q

What are gametes?

A

Gametes are an organism’s reproductive cells. They are also referred to as sex cells. Female gametes are called ova or egg cells, and male gametes are called sperm.

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3
Q

What is x-linked dominant inheritance?

A

X-linked dominant inheritance indicates that a gene responsible for a genetic disorder is located on the X chromosome, and only one copy of the allele is sufficient to cause the disorder when inherited from a parent who has the disorder.

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4
Q

What is the particulate hypothesis?

A

The particulate hypothesis was offered by Gregor Mendel who discovered that traits are inherited in discrete units that we now know as genes. Instead of blending, the offspring inherits a version of a gene, called an allele, from each of the parents. Only one allele is expressed depending on a number of factors.

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5
Q

What is a somatic cell?

A

A somatic cell is any cell of the body except sperm and egg cells. Somatic cells are diploid, meaning that they contain two sets of chromosomes, one inherited from each parent.

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6
Q

What is linkage map?

A

A linkage map (also known as a genetic map) is a table for a species or experimental population that shows the position of its known genes or genetic markers relative to each other in terms of recombination frequency, rather than a specific physical distance along each chromosome.

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7
Q

What is mitosis?

A

Mitosis is a process where a single cell divides into two identical daughter cells (cell division).

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8
Q

What is meiosis?

A

Meiosis is a process where a single cell divides twice to produce four cells containing half the original amount of genetic information. These cells are our sex cells – sperm in males, eggs in females

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9
Q

What is translocation?

A

Translocation is a type of chromosomal abnormality in which a chromosome breaks and a portion of it reattaches to a different chromosome. Chromosomal translocations can be detected by analyzing karyotypes of the affected cells.

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10
Q

What is aneuploidy?

A

Aneuploidy is the presence of an abnormal number of chromosomes in a cell, for example a human cell having 45 or 47 chromosomes instead of the usual 46. It does not include a difference of one or more complete sets of chromosomes.

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