« previous next »

Author Question: An inversion in a human chromosome often results in no demonstrable phenotypic e (Read 621 times)

Hungry!

  • Hero Member
  • *****
  • Posts: 1,071
on: Jun 21, 2013
An inversion in a human chromosome often results in no demonstrable phenotypic effect in the individual. What else may occur?
A) There may be deletions later in life.
B) Some abnormal gametes may be formed.
C) There is an increased frequency of mutation.
D) All inverted chromosomes are deleted.
E) The individual is more likely to get cancer.


camila

  • Hero Member
  • *****
  • Posts: 705
Reply #1 on: Jun 22, 2013
100% it's B, don't forget to gimmi a thumbs up :D


Related Topics

Need homework help now?

Ask unlimited questions for free

Ask a Question

Hungry!

  • Hero Member
  • *****
  • Posts: 1,071
Reply #2 on: Aug 13, 2013
Thanks so much, you were right on.


« previous next »
 

Did you know?

Coca-Cola originally used coca leaves and caffeine from the African kola nut. It was advertised as a therapeutic agent and "pickerupper." Eventually, its formulation was changed, and the coca leaves were removed because of the effects of regulation on cocaine-related products.

Did you know?

Cyanide works by making the human body unable to use oxygen.

Did you know?

Thyroid conditions may make getting pregnant impossible.

Did you know?

Drug-induced pharmacodynamic effects manifested in older adults include drug-induced renal toxicity, which can be a major factor when these adults are experiencing other kidney problems.

Did you know?

Between 1999 and 2012, American adults with high total cholesterol decreased from 18.3% to 12.9%

Human Evolution Human Evolution
A comparison of the proteomes in human liver and skeletal muscle cells A comparison of the proteomes in human liver and skeletal muscle cells
Major structures of the human brain. Major structures of the human brain.
Cross-section view of the human eye. Cross-section view of the human eye.
Segregation of two genetic markers, lying on separate chromosomes (top) or on the same chromosome Segregation of two genetic markers, lying on separate chromosomes (top) or on the same chromosome
A transgenic mouse carrying a mutation in the human SOD1 gene that causes paralysis of the limbs. In A transgenic mouse carrying a mutation in the human SOD1 gene that causes paralysis of the limbs. In
Video: Coaductile pathway, Timing of contraction signal & Conduction system and ECG

For a complete list of videos, visit our video library