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41 Cards in this Set

  • Front
  • Back

Gamete

A reproductive cell

Zygote

The single cell formed from the union of two gametes, a sperm and an ovum.

Deoxyribonucleic acid (DNA)

The chemical composition of the molecules that contain the genes.

Chromosome

One of the 46 molecules of DNA (in 23 pairs) that virtually each cell of the human body contains and that, together, contain the genes.

Gene

A small section of a chromosome; the basic unit for the transmission of heredity.

Allele

A variation that makes a gene different in some way from other genes for the same characteristics.

Cell

Nucleus

Chromosome

DNA molecule

Epigenetics

The study of how environmental factors affect genes and genetic expression.

Genome

The full set of genes that are the instructions to make an individual member of a certain species.

Genotype

An organism's entire genetic inheritance, or genetic potential.

Homozygous

Referring to two genes of one pair that are exactly the same in every letter of their code.

Heterozygous

Referring to two genes of one pair that differ in some way.

23rd pair

The chromosome pair that, in humans, determines the sex.

XY

A 23rd chromosome pair that consists of an X-shaped chromosome from the mother and a Y-shaped chromosome from the father. XY zygotes become male.

XX

A 23rd chromosome pair that consists of two X-shaped chromosomes, one each from the mother and the father. XX zygotes become female.

How many pairs of chromosomes and how many genes does a person usually have?

23 pairs of chromosomes (46 in all)


20,000 genes

What causes the similarities of all humans?

All humans have most of the same genes with identical codes.

Why do two sisters or two brothers in the same family differ genetically?

Some alleles from the father differ from the alleles from the mother, their combination produces a zygote unlike either parent. Thus each new person is a product of two parents but unlike either one.

Which is more important for a person's daily life, the phenotype or genotype, and why?

Phenotype because it is the set of observable characteristics of an individual resulting from the interaction of its genotype with the environment

What determines whether a baby will be a boy or a girl?

23rd chromosome pair.

Stem cells

Cells from which any other specialized type of cell can form.

Monozygotic (MZ) twins

Twins who originate from one zygote that splits apart very early in development. (Identical twins)

Dizygotic (DZ) twins

Twins who are formed when two separate ova are fertilized by two separate sperm at roughly the same time. (Fraternal twins)

Assisted reproductive technology (ART)

A general term for the techniques designed to help infertile couples conceive and then sustain a pregnancy.

In vitro fertilization (IVF)

Fertilization that takes place outside a woman's body (as in a glass laboratory dish)

Intra-cytoplasmic sperm injection (ICSI)

An in vitro fertilization technique in which a single sperm cell is injected directly into an ovum.

How does differentiation affect stem cells?

In differentiation, cells specialize, taking different forms and reproducing at various rates depending on where they are located.

What are the advantages and disadvantages of being a monozygotic twin?

Advantages: Donate an organ to their twin with no organ rejection


What ART measures help a woman who is infertile?

A woman can take a drug, clomid, to cause ovulation.

What ART measures help a man who is infertile?

The woman can be inseminated with another man's sperm.

Phenotype

The observable characteristics of a person, including appearance, personality, intelligence, and all other traits.

Polygenic

Referring to a trait that is influenced by many genes.

Multifactorial

Referring to a trait that is affected by many factors, both genetic and environmental.

Human genome project

An international effort to map the complete human genetic code

Dominant- recessive pattern

The interaction of a heterozygous pair of alleles in such a way that the phenotype reflects one allele more than the other.

Carrier

A person whose genotype includes a gene that is not expressed in the phenotype.

X-linked

A gene carried on the X chromosome.

Copy number variation

Genes with various repeats or deletions of base pairs.