High resolution X chromosome-specific array-CGH detects new CNVs in infertile males
about
Epigenetics and male reproduction: the consequences of paternal lifestyle on fertility, embryo development, and children lifetime healthThe human RHOX gene cluster: target genes and functional analysis of gene variants in infertile menX chromosome-linked CNVs in male infertility: discovery of overall duplication load and recurrent, patient-specific gains with potential clinical relevance.Genetic susceptibility to male infertility: news from genome-wide association studies.Bringing epigenetics into the diagnostics of the andrology laboratory: challenges and perspectives.Male Reproductive Disorders and Fertility Trends: Influences of Environment and Genetic Susceptibility.Human spermatogenic failure purges deleterious mutation load from the autosomes and both sex chromosomes, including the gene DMRT1.Genomic and genetic variation in E2F transcription factor-1 in men with nonobstructive azoospermia.The Genetics of Infertility: Current Status of the Field.Copy number gain of VCX, X-linked multi-copy gene, leads to cell proliferation and apoptosis during spermatogenesis.Initiative for standardization of reporting genetics of male infertility.Single gene defects leading to sperm quantitative anomalies.A Comprehensive Guide to the MAGE Family of Ubiquitin Ligases.Spermatogenic failure and the Y chromosome.Semen quality of young adult ICSI offspring: the first results.Recurrent deletions of the X chromosome linked CNV64, CNV67, and CNV69 shows geographic differences across China and no association with idiopathic infertility in men.Sertoli Cell-Only Syndrome: Behind the Genetic Scenes.RHOXF2 gene, a new candidate gene for spermatogenesis failure.Management of non-obstructive azoospermia.Lessons learned in andrology: from endocrinology to andrology and backwards: the round trip of a clinician.Next-generation sequencing for patients with non-obstructive azoospermia: implications for significant roles of monogenic/oligogenic mutations.A no-stop mutation in MAGEB4 is a possible cause of rare X-linked azoospermia and oligozoospermia in a consanguineous Turkish family.Evidence for the involvement of the proximal copy of the MAGEA9 gene in Xq28-linked CNV67 specific to spermatogenic failure.Karyotype analysis in large sample cases from Shenyang Women's and Children's hospital: a study of 16,294 male infertility patients.Novel biomarker ZCCHC13 revealed by integrating DNA methylation and mRNA expression data in non-obstructive azoospermia.The Klinefelter syndrome is associated with high recurrence of copy number variations on the X chromosome with a potential role in the clinical phenotype.Copy number variations in testicular maturation arrest.Advances in understanding the genetics underlying male infertility and evolving diagnostic and treatment optionsRecurrent X chromosome-linked deletions: discovery of new genetic factors in male infertility
P2860
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P2860
High resolution X chromosome-specific array-CGH detects new CNVs in infertile males
description
2012 nî lūn-bûn
@nan
2012 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
name
High resolution X chromosome-specific array-CGH detects new CNVs in infertile males
@ast
High resolution X chromosome-specific array-CGH detects new CNVs in infertile males
@en
High resolution X chromosome-specific array-CGH detects new CNVs in infertile males
@nl
type
label
High resolution X chromosome-specific array-CGH detects new CNVs in infertile males
@ast
High resolution X chromosome-specific array-CGH detects new CNVs in infertile males
@en
High resolution X chromosome-specific array-CGH detects new CNVs in infertile males
@nl
prefLabel
High resolution X chromosome-specific array-CGH detects new CNVs in infertile males
@ast
High resolution X chromosome-specific array-CGH detects new CNVs in infertile males
@en
High resolution X chromosome-specific array-CGH detects new CNVs in infertile males
@nl
P2093
P2860
P50
P1433
P1476
High resolution X chromosome-specific array-CGH detects new CNVs in infertile males
@en
P2093
Chiara Chianese
Claudia Giachini
Deborah Lo Giacco
Eduard Ruiz-Castane
Fabrice Daguin
P2860
P304
P356
10.1371/JOURNAL.PONE.0044887
P407
P577
2012-10-09T00:00:00Z