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Chromosome 13 is a vital component of the human genome, harboring numerous genes crucial for various biological functions. This analysis explores the genomic structure of Chromosome 13, focusing on its specific loci, including p and q arms, and their implications for genetic research and disease. Understanding the roles of genes located at critical positions (such as 13.12.p and 21.1.q) can provide insights into hereditary conditions and potential therapeutic targets. Further research on this chromosome will enhance our comprehension of genetic variation and chromosomal disorders.
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Chromosome 13 13 12 p 11.2 11.1 11 12.1 12.2 12.3 13 14.1 14.2 14.3 21.1 21.2 q 21.3 22 31 32 33 34