Exam: Genetics Flashcards

1
Q

What are the gs cell theory states

A

All living things are composed of one or more cells
All cells come from or existing cells
Cells are the simplest unit of living organisms

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2
Q

Difference between chromatin, chromatid, centromere

A

Chromatin - DNA
Chromatid - half a chromosome
Centreomete - holding chromatids together

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3
Q

What are the three stages of interphase

A

G1- majour phase of growth
S - DNA replication
G2 - secondary growth phase

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4
Q

Mitosis: describe PMAT

A

Prophase: everything is getting ready to split
Metaphase: all chromosomes go in the middle
Anaphase: split into sister chromatids
Telophase: Chromosomes reach opposite poles of cell and unravel

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5
Q

What is cytokinesis

A

Takes place after telophase, equal division of cytoplasm and organelles among daughter cells and forms a cleavage furrow.

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6
Q

How many chromosomes do we have in our body

A

46 (22 diploids, 2 sex)

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7
Q

What is meiosis

A

Basically mitosis but interkinase only happens once and first it’s diploids then turns into haploids. 4 divisions instead of 2

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8
Q

Purpose of mitosis

A

To grow, Regenerate and maintenance. This takes place throughout life in the somatic cells

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9
Q

Purpose of meiosis

A

To produce gametes with each of of parents genetics .Takes place during puberty in the gamete cells.

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10
Q

What is abnormal meiosis

A

Chances in number or structure

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11
Q

What is deletion in a chromosome

A

A piece of chromosome is lost

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12
Q

What is duplication in chromosome

A

Section of a chromosome appears two or more times in a row

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13
Q

What is Inversion in a chromosome

A

Segment of DNA in a chromosome flips upside down, no information is lost

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14
Q

What is translocation in a chromosome

A

Non homologous chromosomes cross over

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15
Q

What is nondisjunction

A

Improper separation or a fail to separate during meiosis

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16
Q

When does non disjunction happens

A

Anaphase I or Anaphase II.

17
Q

What are the two results on nondisjunction

A

Monosomy= single pair
Trisomy= three pairs

18
Q

What is Trisomy 21

A

Down syndrome

19
Q

What is Trisomy 18

A

Edward syndrome,

20
Q

Trisomy 13

A

Patan syndrome

21
Q

What is XXY

A

Kilnefelter (can’t produce sperm)

22
Q

What is XYY

A

Jacobs (taller than average)

23
Q

What is XXX

A

Triple X (tall and thin with irregular mentrual cycle)

24
Q

What is XO

A

Turner (short statue, webbed feet, sexually underdeveloped)

25
Q

What is a ultrasound

A

Non invasive Visual image of body through sound waves

26
Q

What is a multiple marker screen

A

Non invasive Blood test and ultrasound at 15-20 weeks. Check mothers blood for tube defects. Tests 21 and 18

27
Q

What is Aminocentesis

A

Inavise needle to uteri’s to extract amniotic fluid. 1% chance of miscarriage. Tests everything.

28
Q

What is chorionic villi sampling

A

Invasive sampling of placenta to take out chorionic villi. 1% miscarriage. Tests for everything

29
Q

What is a genotype

A

The genetic combination of a gene

30
Q

What is a phenotype

A

Things seen visually on a person

31
Q

What is true breeding

A

When parents give homologous traits to the child