AZFc deletions and spermatogenic failure: a population-based survey of 20,000 Y chromosomes.
about
Epigenetics and male reproduction: the consequences of paternal lifestyle on fertility, embryo development, and children lifetime healthMicroarray Analysis of Copy Number Variants on the Human Y Chromosome Reveals Novel and Frequent Duplications Overrepresented in Specific HaplogroupsWhole-genome sequencing in health care. Recommendations of the European Society of Human Genetics.Clinical relevance of Y-linked CNV screening in male infertility: new insights based on the 8-year experience of a diagnostic genetic laboratoryHuman Y chromosome copy number variation in the next generation sequencing era and beyond.Male Reproductive Disorders and Fertility Trends: Influences of Environment and Genetic Susceptibility.Insights on the functional impact of microRNAs present in autism-associated copy number variants.Copy number variations of the extensively amplified Y-linked genes, HSFY and ZNF280BY, in cattle and their association with male reproductive traits in Holstein bulls.Screening for AZFc partial deletions in Dravidian men with nonobstructive azoospermia and oligozoospermia.Common AZFc structure may possess the optimal spermatogenesis efficiency relative to the rearranged structures mediated by non-allele homologous recombination.Copy number variation in the human Y chromosome in the UK population.Susceptibility of gr/gr rearrangements to azoospermia or oligozoospermia is dependent on DAZ and CDY1 gene copy deletions.Discrimination of Deletion and Duplication Subtypes of the Deleted in Azoospermia Gene Family in the Context of Frequent Interloci Gene Conversion.Multiplex PCR based screening for micro/partial deletions in the AZF region of Y-chromosome in severe oligozoospermic and azoospermic infertile men in IranA Screen for Genomic Disorders of Infertility Identifies MAST2 Duplications Associated with Nonobstructive Azoospermia in Humans.Gr/gr deletions on Y-chromosome correlate with male infertility: an original study, meta-analyses, and trial sequential analysesFISH and array CGH characterization of de novo derivative Y chromosome (Yq duplication and partial Yp deletion) in an azoospermic male.Novel Y-chromosomal microdeletions associated with non-obstructive azoospermia uncovered by high throughput sequencing of sequence-tagged sites (STSs).Y-Chromosome Structural Diversity in the Bonobo and Chimpanzee LineagesEpigenetic regulation of the RHOX homeobox gene cluster and its association with human male infertility.Human Y-chromosome variation in the genome-sequencing era.Single gene defects leading to sperm quantitative anomalies.Partial Deletions of Y-Chromosome in Infertile Men with Non-obstructive Azoospermia and Oligoasthenoteratozoospermia in a Turkish Population.Copy-number variations in Y-chromosomal azoospermia factor regions identified by multiplex ligation-dependent probe amplification.Y chromosome palindromes and gene conversion.Spermatogenic failure and the Y chromosome.Genome-wide Loci linked to non-obstructive azoospermia susceptibility may be independent of reduced sperm production in males with normozoospermia.The diagnosis of male infertility: an analysis of the evidence to support the development of global WHO guidance-challenges and future research opportunities.First line fertility treatment strategies regarding IUI and IVF require clinical evidence.Azoospermia Factor C Subregion of the Y Chromosome.Genetics of the human Y chromosome and its association with male infertility.Copy number variation of functional RBMY1 is associated with sperm motility: an azoospermia factor-linked candidate for asthenozoospermia.Evidence for the involvement of the proximal copy of the MAGEA9 gene in Xq28-linked CNV67 specific to spermatogenic failure.High Levels of Copy Number Variation of Ampliconic Genes across Major Human Y Haplogroups.Current issues in medically assisted reproduction and genetics in Europe: research, clinical practice, ethics, legal issues and policy
P2860
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P2860
AZFc deletions and spermatogenic failure: a population-based survey of 20,000 Y chromosomes.
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年学术文章
@wuu
2012年学术文章
@zh-cn
2012年学术文章
@zh-hans
2012年学术文章
@zh-my
2012年学术文章
@zh-sg
2012年學術文章
@yue
name
AZFc deletions and spermatogen ...... urvey of 20,000 Y chromosomes.
@ast
AZFc deletions and spermatogen ...... urvey of 20,000 Y chromosomes.
@en
AZFc deletions and spermatogen ...... urvey of 20,000 Y chromosomes.
@nl
type
label
AZFc deletions and spermatogen ...... urvey of 20,000 Y chromosomes.
@ast
AZFc deletions and spermatogen ...... urvey of 20,000 Y chromosomes.
@en
AZFc deletions and spermatogen ...... urvey of 20,000 Y chromosomes.
@nl
altLabel
AZFc deletions and spermatogen ...... survey of 20,000 Y chromosomes
@en
prefLabel
AZFc deletions and spermatogen ...... urvey of 20,000 Y chromosomes.
@ast
AZFc deletions and spermatogen ...... urvey of 20,000 Y chromosomes.
@en
AZFc deletions and spermatogen ...... urvey of 20,000 Y chromosomes.
@nl
P2093
P2860
P50
P1476
AZFc deletions and spermatogen ...... urvey of 20,000 Y chromosomes.
@en
P2093
David C Page
Helen Skaletsky
Janet D Marszalek
Kathryn Irenze
Laura G Brown
Sherman J Silber
P2860
P304
P356
10.1016/J.AJHG.2012.09.003
P407
P577
2012-10-25T00:00:00Z