This topic contains a solution. Click here to go to the answer
« previous next »

Author Question: The gene responsible for the fragile X syndrome is __________. A. FRMP B. FMR1 C. FXS1 D. ... (Read 79 times)

maychende

  • Hero Member
  • *****
  • Posts: 556
on: Jun 25, 2018
The gene responsible for the fragile X syndrome is __________.
 
  A. FRMP
  B. FMR1
  C. FXS1
  D. FRM1

Question 2

__________ is an inflammation of the lung.
 
  A. Tuberculosis
  B. Pneumonia
  C. Atelectasis
  D. Bronchiectasis


Related Topics

Need homework help now?

Ask unlimited questions for free

Ask a Question
Marked as best answer by a Subject Expert

31809pancho

  • Sr. Member
  • ****
  • Posts: 317
Reply #1 on: Jun 25, 2018
Answer to Question 1

B

Answer to Question 2

B


maychende

  • Member
  • Posts: 556
Reply 2 on: Jun 25, 2018
Gracias!

epscape

  • Member
  • Posts: 335
Reply 3 on: Yesterday
:D TYSM

« previous next »
 

Did you know?

Astigmatism is the most common vision problem. It may accompany nearsightedness or farsightedness. It is usually caused by an irregularly shaped cornea, but sometimes it is the result of an irregularly shaped lens. Either type can be corrected by eyeglasses, contact lenses, or refractive surgery.

Did you know?

Adult head lice are gray, about ? inch long, and often have a tiny dot on their backs. A female can lay between 50 and 150 eggs within the several weeks that she is alive. They feed on human blood.

Did you know?

People about to have surgery must tell their health care providers about all supplements they take.

Did you know?

Bacteria have flourished on the earth for over three billion years. They were the first life forms on the planet.

Did you know?

Fewer than 10% of babies are born on their exact due dates, 50% are born within 1 week of the due date, and 90% are born within 2 weeks of the date.

Gene Therapy Gene Therapy
Inheritance Pattern for the Mutated FOXP2 Gene in the KE Family Inheritance Pattern for the Mutated FOXP2 Gene in the KE Family
A deletion of part of chromosome 5 is associated with cri du chat syndrome. By comparing the region A deletion of part of chromosome 5 is associated with cri du chat syndrome. By comparing the region
An endoscopic view of the colon of someone who carries the normal alleles for the APC gene An endoscopic view of the colon of someone who carries the normal alleles for the APC gene
Gene structure Gene structure
The X/A ratio determines gene transcription and transcript splicing pattern The X/A ratio determines gene transcription and transcript splicing pattern
Video: Baroreceptor Reflex

For a complete list of videos, visit our video library