Human genome, around three billion sets of deoxyribonucleic corrosive (DNA) bases that make up the association of chromosomes of the human body. The human genome incorporates the DNA coding districts (somewhere in the range of 20,000 and 25,000) of the human life form, just as the non-coding areas of DNA, which don't encode any quality. In 2003 the DNA succession of the whole human genome was known. The human genome, similar to the genomes of all other living creatures, is an assortment of long DNA polymers. These polymers are kept in copy duplicate as chromosomes in every human cell and encode in their grouping of constituent bases (guanine [G], adenine [A], thymine [T] and cytosine [C]) the subtleties of the sub-atomic attributes and physical that relates to the comparing life form. The succession of these polymers, their association and structure and the substance changes that contain not just the apparatuses important to communicate the data contained in the genome, yet additionally with the genome the capacity to duplicate, use, bundle and in any case look after itself.
Thesis: Human Genetics & Embryology
Thesis: Human Genetics & Embryology
Scientific Tracks Abstracts: Molecular and Genetic Medicine
Scientific Tracks Abstracts: Molecular and Genetic Medicine
Scientific Tracks Abstracts: Journal of Tissue Science and Engineering
Scientific Tracks Abstracts: Journal of Tissue Science and Engineering
Accepted Abstracts: Journal of Tissue Science and Engineering
Accepted Abstracts: Journal of Tissue Science and Engineering
Scientific Tracks Abstracts: Molecular Biology: Open Access
Scientific Tracks Abstracts: Molecular Biology: Open Access
Scientific Tracks Abstracts: Journal of Cytology & Histology
Scientific Tracks Abstracts: Journal of Cytology & Histology
Human Genetics & Embryology received 309 citations as per Google Scholar report
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