Chromosome 22

Chromosome 22 is one of the 23 pairs of chromosomes that contain the human genome. It is the second-smallest human chromosome, spanning about 49 million base pairs, making it one of the smallest pieces of genetic material in the human body. Chromosome 22 plays an important role in human development and can be used to identify genetic disorders and cancer. Genetic abnormalities on Chromosome 22 have been linked to schizophrenia, autism, and several forms of cancer, making it an important area of further research. Chromosome 22 is also associated with the regulation of many genes involved in the development of the central nervous system, making it a key factor in understanding the pathogenesis of neurological diseases.

← Journal of Chromosomes

Related Articles

6 article(s) found

Pericentric Inversion in Chromosome 10 in a Girl, Inherited from a Phenotypically Normal Mother: Case Report and Literature Review

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Humans Chromosome 1 Fractal Periods Signature is Highly Correlated with Intelligence and Brain Evolution

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Intriguing Humans and Primates chromosomes 4

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An Inherited Balanced Translocation Between Chromosomes 4 and 6 in Recurrent Pregnancy Loss: A Case Report

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A Patient with Monoclonal Gammopathy of Undetermined Significance and Detected Philadelphia Chromosome

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The Chromosomes of Dictyostelium Giganteum

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