Characterization and Association of Marker Chromosomes with Male Infertility
Dong Suk Kim,Sang Hee Park,Sung Han Shim,Dae Keun Kim,Sang Woo Lyu,Ji Won Kim,Woo Sik Lee,Seung-Hun Song +7 more
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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.About:
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.read more
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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
Alberto Ferlin,Florina Raicu,Valentina Gatta,Daniela Zuccarello,Giandomenico Palka,Carlo Foresta +5 more
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.
Thomas Liehr,Anja Weise +1 more
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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