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Open AccessJournal ArticleDOI

Characterization and Association of Marker Chromosomes with Male Infertility

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TLDR
A molecular cytogenetic characterization of small supernumerary marker chromosome (sSMCs) was performed and their association with male infertility was investigated to characterize and identify the origin of their marker chromosome.
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This article is published in Journal of Men's Health.The article was published on 2020-07-17 and is currently open access. It has received 0 citations till now. The article focuses on the topics: Marker chromosome & Small supernumerary marker chromosome.

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References
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Journal ArticleDOI

The genetic causes of male factor infertility: A review

TL;DR: Analysis of the genetic factors that impact male factor infertility will provide valuable insights into the creation of targeted treatments for patients and the determination of the causes of idiopathic infertility.
Journal ArticleDOI

Male infertility: role of genetic background

TL;DR: The genetic causes of male infertility known to date, the genetic polymorphisms possibly associated with male infertility, and novel results of global gene expression profiling of normal human testis by microarray technology are reported.
Journal ArticleDOI

Small supernumerary marker chromosomes (sSMC) in humans.

TL;DR: An overview of small supernumerary marker chromosomes is presented, including the first attempt to address problems of nomenclature and their modes of formation, problems connected with mosaicism plus familial occurrence and a short review of the up-to-date approaches available for sSMC characterization.
Journal ArticleDOI

Frequency of small supernumerary marker chromosomes in prenatal, newborn, developmentally retarded and infertility diagnostics.

TL;DR: There is a strong need for a better genotype-phenotype correlation enabling better genetic counseling and no increased risk for the presence of sSMC was detected in ICSI-induced pregnancies.
Journal ArticleDOI

Genome-wide study of single-nucleotide polymorphisms associated with azoospermia and severe oligozoospermia.

TL;DR: This pilot genome-wide association study employed genotyping microarray technology to interrogate over 370,000 single-nucleotide polymorphisms (SNPs) in men with azoospermia and severe oligozoospermia, along with normozoospermic controls, in an effort to discover novel genetic variants significantly associated with male infertility.
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