Chromosome Mutations

Chromosome mutations are changes in the number or structure of chromosomes, which can occur naturally or as a result of exposure to certain environmental agents. Mutations can cause diseases, such as Down syndrome, where an extra chromosome 21 is present, or Turner syndrome, where one of the two X chromosomes is missing. Other types of mutations can also lead to abnormalities in an organism's physical or mental characteristics. Chromosome mutations are important to understand in order to diagnose and treat genetic diseases, and can provide valuable insight into the evolution of species.

← Journal of Chromosomes

Related Articles

10 article(s) found

The Identification of Somatic Mutations in Interferon-G Signal Molecules in Human Uterine Leiomyosarcoma

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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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Characterization of rpoB Gene Mutations Associated with Rifampicin Resistance in Multidrug Resistant Tuberculosis Patients Co-infected with HIV from Southern India.

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An Algorithm to Predict the Possible SARS-CoV-2 Mutations

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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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Understanding Inherited Bleeding Disorders: Genetic Mutations in Blood Coagulation Factors and Regulatory Proteins

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