Genetic Disorders in Iraqi population, Detection and causes
| AUTHOR | Al-Hassani, Dr Owayes Mouaffaq |
| PUBLISHER | LAP Lambert Academic Publishing (10/17/2019) |
| PRODUCT TYPE | Paperback (Paperback) |
Description
A genetic disorder is a genetic problem caused by one or more abnormalities formed in the genome. Most genetic disorders are quite rare and affect one person in every several thousands or millions. ... Genetic disorders may be hereditary or non-hereditary, meaning that they are passed down from the parents' genes.The sequence of the human genome is providing us with the first holistic view of our genetic heritage. While not yet complete, continued refinement of the data bring us ever closer to a complete human genome reference sequence. This will be a fundamental resource in future biomedical research.The 46 human chromosomes (22 pairs of autosomal chromosomes and 2 sex chromosomes) between them house almost 3 billion base pairs of DNA that contains about 30,000 - 40,000 protein-coding genes. The coding regions make up less than 5% of the genome (the function of the remaining DNA is not clear) and some chromosomes have a higher density of genes than others.Most of the genetic disorders featured on this web site are the direct result of a mutation in one gene.
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Product Format
Product Details
ISBN-13:
9786200442413
ISBN-10:
620044241X
Binding:
Paperback or Softback (Trade Paperback (Us))
Content Language:
English
More Product Details
Page Count:
92
Carton Quantity:
76
Product Dimensions:
6.00 x 0.22 x 9.00 inches
Weight:
0.32 pound(s)
Country of Origin:
US
Subject Information
BISAC Categories
Science | Life Sciences - Genetics & Genomics
Descriptions, Reviews, Etc.
publisher marketing
A genetic disorder is a genetic problem caused by one or more abnormalities formed in the genome. Most genetic disorders are quite rare and affect one person in every several thousands or millions. ... Genetic disorders may be hereditary or non-hereditary, meaning that they are passed down from the parents' genes.The sequence of the human genome is providing us with the first holistic view of our genetic heritage. While not yet complete, continued refinement of the data bring us ever closer to a complete human genome reference sequence. This will be a fundamental resource in future biomedical research.The 46 human chromosomes (22 pairs of autosomal chromosomes and 2 sex chromosomes) between them house almost 3 billion base pairs of DNA that contains about 30,000 - 40,000 protein-coding genes. The coding regions make up less than 5% of the genome (the function of the remaining DNA is not clear) and some chromosomes have a higher density of genes than others.Most of the genetic disorders featured on this web site are the direct result of a mutation in one gene.
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