GENES AND HEREDITY Flashcards

1
Q

the transmission of traits and/or disorder of parents to their offspring through genetic mechanisms- half paternal, half materna

A

HEREDITY

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2
Q

states that one trait has the capacity to suppress recessive trait; dominant trait are usually physiological.

A

PRINCIPLE OF DOMINANCE

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3
Q

trait that appear only in the absence of dominance; not express because dominant trait/ gene is present.

A

PRINCIPLE OF RECESSIVE

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4
Q

are units of hereditary material contained in a person’s cell; hold information for all aspects of bodily growth and development.

A

GENES

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5
Q

segments of DNA(deoxyribonucleic acid) within chromosomes.

A

GENES

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6
Q

contains a long strand of the hereditary substance deoxyribonucleic acid(DNA)

A

CHROMOSOMES

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7
Q

males gamete

A

SPERM

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8
Q

females gamete

A

OVUM

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9
Q

human reproduction cells which are created in the testes of male and ovary of the female

A

GAMETE

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10
Q

begins with the fertilization of a female’s gamete by a male’s gamete.

A

REPRODUCTION

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11
Q

union of sperm and the ovum; it occurs when the head of the sperm penetrates a mature ovum.

A

FERTILIZATION

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12
Q

single cell formed through fertilization; 2 set of unpaired chromosome

A

ZYGOTE

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13
Q

how many y

A

23

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14
Q

how many x

A

23

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15
Q

total of chromosomes

A

46

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16
Q

an individual’s genetic heritage, it is the actual genetic material.

A

GENOTYPE

17
Q

This includes an individual’s physical and psychological characteristics.

A

PHENOTYPE

18
Q

a process of fertilization in which a man’s sperm is placed directly into a woman’s vagina by a physician

A

ARTIFICIAL INSEMINATION

19
Q

a procedure in which a woman’s ova are removed from her ovaries and a man’s sperm are used to fertilize the ova in a laboratory.

A

IN VITRO FERTILIZATION (IVF)

20
Q

High-frequency sound waves directed at the mother’s abdomen produce a picture of the fetus in the uterus

A

Ultrasound (sonogram)

20
Q

uses high frequency transvaginal probes & digital image processing to produce a picture of the embryo in the uterus.

A

Sonoembryology

21
Q

prenatal diagnostic technique that uses a syringe to withdraw a sample of amniotic fluid through the mother’s abdomen.

A

Amniocentesis

22
Q

prenatal diagnostic technique that involves taking a sample of tissue from the chorion, extracted from the placenta through the vagina

A

Chorionic villus sampling

23
Q

Tiny viewing scope is inserted in the woman’s abdomen to view the embryo or fetus.

A

Embryoscopy

24
Q

can assist in diagnosis of non-chromosomal genetic disorders.

A

Fetoscopy

25
Q

a recessive hereditary disorder of protein metabolism. The basic defect is the absence of enzymes necessary to metabolize.

A

PHENYLKETONURIA (PKU)

26
Q

an amino acid that is present in many foods ;the brain is damaged by an enormous build up of phenylalanine leading to mental retardation.

A

phenylalanine

27
Q

originally named “mongolism” common form of cognitive disorder due to the presence of extra chromosome 21, for a total of 3 rather than the typical 2 copies making it 47 instead or normal 46

A

DOWN SYNDROME

28
Q

the disorder is also called trisomy 21

A

DOWN SYNDROME

29
Q

most frequent cause of inherited mental retardation ; the long arm of the X chromosome is prone to breaking for the DNA there is unstable.

A

FRAGILE X SYNDROME