The origin, mechanisms, incidence and clinical consequences of chromosomal mosaicism in humans. - Wikidata - wikimedia - TriplyDB

The origin, mechanisms, incidence and clinical consequences of chromosomal mosaicism in humans.

The origin, mechanisms, incidence and clinical consequences of chromosomal mosaicism in humans.

http://www.wikidata.org/entity/Q34411991

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Unrevealed mosaicism in the next-generation sequencing era Somatic mosaicism in the human genome Detecting mosaicism in trophectoderm biopsies: current challenges and future possibilities The accumulation of vitrified oocytes is a strategy to increase the number of euploid available blastocysts for transfer after preimplantation genetic testing.Birth of a child with trisomy 9 mosaicism syndrome associated with paternal isodisomy 9: case of a positive noninvasive prenatal test result unconfirmed by invasive prenatal diagnosis.Evidence of Selection against Complex Mitotic-Origin Aneuploidy during Preimplantation Development Irregular cleavage of early preimplantation human embryos: characteristics of patients and pregnancy outcomes.Micronucleus formation causes perpetual unilateral chromosome inheritance in mouse embryos.FISH and array CGH characterization of de novo derivative Y chromosome (Yq duplication and partial Yp deletion) in an azoospermic male.Abnormally cleaving embryos are able to produce live births: a time-lapse study.Molecular analysis of DNA in blastocoele fluid using next-generation sequencing.Noninvasive chromosome screening of human embryos by genome sequencing of embryo culture medium for in vitro fertilization.A randomized and blinded comparison of qPCR and NGS-based detection of aneuploidy in a cell line mixture model of blastocyst biopsy mosaicism Is the hypothesis of preimplantation genetic screening (PGS) still supportable? A review.Diagnosis of human preimplantation embryo viability.Pre-implantation genetic diagnosis and screening: now and the future.Evaluation of comprehensive chromosome screening platforms for the detection of mosaic segmental aneuploidy Mosaicism in health and disease - clones picking up speed.Physiological Aspects of Female Fertility: Role of the Environment, Modern Lifestyle, and Genetics.Nuclear and mitochondrial DNA in blastocoele fluid and embryo culture medium: evidence and potential clinical use.Human embryo mosaicism: did we drop the ball on chromosomal testing?First trimester pregnancy loss: Clinical implications of genetic testing.Hatching status before embryo transfer is not correlated with implantation rate in chromosomally screened blastocysts.Unrecognized viral infections and chromosome abnormalities as a cause of fetal death - examination with fluorescence in situ hybridization, immunohistochemistry and polymerase chain reaction.Should preimplantation genetic screening (PGS) be implemented to routine IVF practice?Phenotypic extremes in liveborn monozygotic twins with mosaic Edwards syndrome.Environmental Impact on Reproductive Health: Can Biomarkers Offer Any Help?Assisted reproductive technology (ART) cumulative live birth rates following preimplantation genetic diagnosis for aneuploidy (PGD-A) or morphological assessment of embryos: A cohort analysis.Mosaic embryo transfer after oocyte in vitro maturation in combination with non-invasive prenatal testing (NIPT)-first report of a euploid live birth.Mosaicism: throwing the baby out with the bath water?Robust identification of mosaic variants in congenital heart disease.Human ring chromosome registry for cases in the Chinese population: re-emphasizing Cytogenomic and clinical heterogeneity and reviewing diagnostic and treatment strategies.Detection and quantitation of chromosomal mosaicism in human blastocysts using copy number variation sequencing.First-trimester spontaneous pregnancy loss - molecular analysis using multiplex ligation-dependent probe amplification.Abnormalities in centrosome number in human embryos and embryonic stem cells.Embryonic hypocellularity, blastogenetic malformations, and fetal growth restriction.Behavioral Variability and Somatic Mosaicism: A Cytogenomic Hypothesis.Clinical reassessment of human embryo ploidy status between cleavage and blastocyst stage by Next Generation Sequencing

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The origin, mechanisms, incidence and clinical consequences of chromosomal mosaicism in humans.

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The origin, mechanisms, incide ...... romosomal mosaicism in humans.

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Human Reproduction Update

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The origin, mechanisms, incide ...... romosomal mosaicism in humans.

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J Michael Wilson

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Molecular cytogenetic detection of confined gonadal mosaicism in a conceptus with trisomy 16 placental mosaicism

Endoreplication and polyploidy: insights into development and disease

Genetic instabilities in human cancers

European collaborative research on mosaicism in CVS (EUCROMIC)--fetal and extrafetal cell lineages in 192 gestations with CVS mosaicism involving single autosomal trisomy

Origin of extraembryonic mesoderm in experimental animals: relevance to chorionic mosaicism in humans

Chromosomal mosaicism confined to the placenta in human conceptions

To err (meiotically) is human: the genesis of human aneuploidy

Spindle abnormalities in normally developing and arrested human preimplantation embryos in vitro identified by confocal laser scanning microscopy.

Germ-line transmission of trisomy 21: Data from 80 families suggest an implication of grandmaternal age and a high frequency of female-specific trisomy rescue.

Chromosome abnormalities in human embryos.

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