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National Journal of Andrology ; (12): 445-448, 2002.
Article in Chinese | WPRIM | ID: wpr-322566

ABSTRACT

About 10%-15% of azoospermic and 5%-10% of severely oligozoospermic men with idiopathic infertility have Yq microdeletions which could be transmitted to their male offspring by means of ICSI. We review present studies about Yq microdeletions including incidence, region, correlations between genotype and phenotype, the mechanism of Yq deletions and try to further understand the cause of male infertility as well as provide a new way for diagnosis and therapy.


Subject(s)
Humans , Male , Chromosome Deletion , Chromosome Mapping , Chromosomes, Human, Y , Genetics , Genotype , Infertility, Male , Genetics , Pathology , Phenotype , Sex Chromosome Aberrations
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