The Role of Genetic Mutations in XX Male Syndrome | Clinical Medicine and Medical Research

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Published Dec 1, 2020

DOI: https://doi.org/10.52845/CMMR/2020v1i2a9

Shahin Asadi

1Medical Genetics-Harvard University. Director of the Division of Medical Genetics and Molecular Optogenetic Research.

Amir Houssein Kiani

2Division of Medical Genetics and Molecular Pathology Research, Harvard University, Boston Children's Hospital

Abstract

The XX male syndrome results from crossover between the X and Y chromosomes outside of the pseudoautosomal region during Meiosis I, which transfers the SRY (sex-determining region) of the Y chromosome to the X chromosome, such that testicular rather than ovarian development occurs.

Keywords

XX Male Syndrome, SRY gene, Y chromosome, X chromosome, Testicular developmental disorder.

References

How to Cite

The Role of Genetic Mutations in XX Male Syndrome. (2020). Clinical Medicine and Medical Research, 1(2), 47-50. https://doi.org/10.52845/CMMR/2020v1i2a9

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Vol. 1 No. 2 (2020)

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Articles

How to Cite

The Role of Genetic Mutations in XX Male Syndrome. (2020). Clinical Medicine and Medical Research, 1(2), 47-50. https://doi.org/10.52845/CMMR/2020v1i2a9

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