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Y chromosome-related genetic diseases / 中华医学遗传学杂志
Chinese Journal of Medical Genetics ; (6): 350-354, 2022.
Artículo en Chino | WPRIM | ID: wpr-928417
ABSTRACT
As a male-specific chromosome, the structure of Y chromosome is complex and lacks of recombination, with numerous repeating, amplifying and palindromic sequences. The research of Y chromosome is difficult and slow since there are few protein coding genes and a large amount of heterochromatin which has caused extreme difficulty for sequencing. In recent years, an increasing number of studies have been focused on the Y chromosome. With the completion of the sequencing of human Y chromosome, the rapid development of sequencing technology, and the composition of DNA sequences in human Y chromosomes and the determination of gene content. This paper has summarized the structural composition and genes function of human Y chromosome, as well as the related hereditary diseases, with an aim to provide reference for Y chromosome-related genetic research.
Asunto(s)
Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Cromosomas Humanos Y Límite: Humanos / Masculino Idioma: Chino Revista: Chinese Journal of Medical Genetics Año: 2022 Tipo del documento: Artículo

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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Cromosomas Humanos Y Límite: Humanos / Masculino Idioma: Chino Revista: Chinese Journal of Medical Genetics Año: 2022 Tipo del documento: Artículo