Chapter 5- Heredity And Disease Flashcards

0
Q

A molecule of DNA found in the human cell. Each human cell contains 46 chromosomes divided into 23 pairs

A

Chromosomes

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1
Q

The blue print for protein synthesis within a cell

A

Deoxyribonucleic acid or DNA

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2
Q

Found in chromosomes, each is responsible for the synthesis of one protein

A

Gene

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3
Q

Name for 44 of the 46 chromosomes; does not include the sex hormones.

A

Autosome

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4
Q

The normal chromosomal composition of the nucleus of the cell that is characteristic of each species.

A

Karyotype

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5
Q

Alternative forms of a gene

A

Allele

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6
Q

A person having the same two alleles of a particular gene

A

Homozygous

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7
Q

A person having two different alleles of a certain gene

A

Heterozygous

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8
Q

A gene that is expressed when inherited

A

Dominant

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9
Q

Term used to describe an allele that manifests itself when the person is homozygous for the trait.

A

Recessive

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10
Q

the genetic makeup of an organism or group of organisms with reference to a single trait, set of traits, or an entire complex of traits.

A

Genotype

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11
Q

the appearance of an organism resulting from the interaction of the genotype and the environment.

A

Phenotype

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12
Q

a specialized structure on the chromosome, appearing during cell division as the constricted central region where the two chromatids are held together and form an X shape.

A

Centromere

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13
Q

a diagram that is used to predict an outcome of a particular cross or breeding experiment

A

Punnett square

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14
Q

Disease that spreads through the family, May or may not be genetic

A

Familial

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15
Q

passing, or capable of passing, naturally from parent to offspring through the genes

A

Hereditary

16
Q

incapable of producing offspring; does not make gametes

A

Sterile

17
Q

A person that cannot have children

Ie) post vasectomy or tubal

A

Infertile

18
Q

Diseases transmitted on the sex chromosome

A

Sex-linked

19
Q

a condensed, inactivated X chromosome present in most female mammals in the nuclei of all cells except the germ cells: used, as in sports competitions, to verify that an individual is genetically female.

A

Barr body

20
Q

Individuals who have both testes and ovaries

A

Hermaphrodite

21
Q

Incorrect # of chromosomes

A

Aneuploidy

22
Q

The failure of two chromosomes to separate as the gametes, either the egg or the sperm are being formed.

A

Nondisjunction

23
Q

The condition of having three copies of chromosome 21; causes Down’s syndrome

A

Trisomy

24
Q

Reordering of genes, three types: shuffling, deletion and addition

A

Gene rearrangement

25
Q

to jumble together, mix, or interchange the positions of chromosomes

A

Shuffling

26
Q

a type of chromosomal aberration in which a segment of the chromosome is removed or lost.

A

Deletion

27
Q

Duplicate genes

A

Addition

28
Q

A diagnostic test for hereditary diseases performed on fetal cells withdrawn from amniotic fluid

A

Amniocentesis

29
Q

Genetic test involving the removal of cells from the villi through the cervix

A

Chorionic villus sampling

30
Q

Diseases that appear at birth or shortly after birth but are not caused by genetic or chromosomal abnormalities

A

Congenital disease

31
Q

Built wrong from the start, fetal alcohol syndrome

A

Deformation

32
Q

Changed after it was built, club feet

A

Malformation

33
Q

test to evaluate health of newborns.

A

Apgar