This website is committed to genetics education awareness. To obtain a better understanding about genetic revolution, we provide the history of genetics. The latest information on all human genetic disorders from Achondroplasia to Wilson's disease is available. Other areas of focus include: dna and rna sequencing, stem cell research and therapy, genetic testing and screening, genetic selection, genes and behavior, mental health, gene therapy, cytocogenetics, pharmacogenetics, xenotransplantation, cloning, ethical, legal, and social issues in medical genetics.


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Archive for April, 2008

Understanding Genetics: Interview 3

Posted by Chavonne Jones On April - 29 - 2008 ADD COMMENTS Subscribe here

Understanding Genetics: Interview 2

Posted by Chavonne Jones On April - 29 - 2008 ADD COMMENTS Subscribe here

Understanding Genetics: Interview 1

Posted by Chavonne Jones On April - 29 - 2008 ADD COMMENTS Subscribe here

Genetics Revision Video

Posted by Chavonne Jones On April - 29 - 2008 ADD COMMENTS Subscribe here

A brief summary of work covered so far in the topic Inheritance and Variation.

Lakshmi Mehta M.D at Mount Sinai Medical Center discusses the roles of recessive and dominant genes.

Hirschsprung Disease

Posted by Chavonne Jones On April - 8 - 2008 1 COMMENT Subscribe here

Hirchsprung’s disease is an abnormality in which certain nerve fibers are absent in segments of the bowel. This disease is caused by certain nerve cells in the large intestine that didn’t develop before birth. Without the nerves, the affected colon lacks the ability to move bowel contents. This disease can affect varying lengths of the bowel segment.

Hirchsprung's Disease affected colon

Hemochromatosis

Posted by Chavonne Jones On April - 8 - 2008 ADD COMMENTS Subscribe here

Hemochromatosis is a genetic disorder that causes the body to increase the absorption of intestinal iron. This iron overload can eventually cause cirrhosis of the liver.

Hemochromatosis affected livers compared to normal liver

Fragile X Syndrome

Posted by Chavonne Jones On April - 8 - 2008 1 COMMENT Subscribe here

Fragile X Syndrome is the most common form of inherited mental retardation. This syndrome is caused by a mutation in the FMR-1 gene on the x chromosome. Individuals with this disorder have developmental delay, variable levels of retardation, behavioral and emotional difficulties, and possible physical traits.

Caucasion boy with Fragile X Asain boy with Fragile X Hispanic boy with Fragile X


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