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Inheritance and Genetics

27 Questions  I  15 Attempts  I  Created By mywickedream 386 days ago
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Question Excerpt From Inheritance and Genetics
Q.1) 

 

 

Fertilization normally occurs within which structure?

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B.
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Q.2) 

 

 

This is a series of functional changes that sperm go through when they are in the female reproductive tract.

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B.
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D.
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Q.3) 

 

 

The fusion of the secondary oocyte and the sperm results in which developmental stage?

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D.
E.
Q.4) 

 

 

This is the part of the blastocyst that promotes implantation and produces hCG.

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E.
Q.5) 

 

 

This is the portion of the endometrium that lays between the embryo and the stratum basalis.

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Q.6) 

 

 

This develops from the epiblast and carries a protective fluid.

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Q.7) 

 

This will become the primary structure for exchange of material between the mother and the fetus.

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D.
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Q.8) 

 

Each somite may differentiate into a

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Q.9) 

 

This is the connection between the placenta and the embryo.

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E.
Q.10) 

 

How many pairs of pharyngeal arches are there?

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B.
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Q.11) 

 

This is any agent or influence that causes developmental defects in an embryo.

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Q.12) 

 

This exam is performed between 14-16 weeks gestation and is used to detect genetic abnormalities.

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Q.13) 

 

CVS is taking cells from where?

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Q.14) 

 

This hormone is secreted by nonpregnant women from secretory cells in the hypothalamus.

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D.
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Q.15) 

 

During pregnancy stroke volume can increase by

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D.
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Q.16) 

 

Labor cannot take place until all of this hormone’s effects are diminished.

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D.
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Q.17) 

 

This is the time from the onset of labor to the complete dilation of the cervix.

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Q.18) 

 

Involution is

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Q.19) 

 

In infants this connects the umbilical vein to the inferior vena cava.

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B.
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E.
Q.20) 

 

This is a principle hormone that releases milk into the mammary ducts.

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D.
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Q.21) 

 

This is a permanent change in an allele.

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Q.22) 

 

When phenotype can be drastically different depending on parental origin it is called:

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B.
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D.
E.
Q.23) 

 

An example of incomplete dominance is

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Q.24) 

 

If one parent has type A blood and one parent has type B blood, what blood type is possible for their child?

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B.
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D.
E.
Q.25) 

 

If a child has B blood, and the mother has B blood, what is the possible genotype of the father?

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B.
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D.
E.
Q.26) 

 

Chromosome #15 is considered

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E.
Q.27) 

 

A Barr body

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B.
C.
D.
E.

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