Chorionic Villus Sampling [PDF]
Seminars in Interventional Radiology, 1992 T W, Meade, A M, Grant
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Chorionic villus-derived mesenchymal stem cell-mediated NRG1 upregulation promotes HTR-8/SVneo cells proliferation through the activation of the NF-κB signaling pathway. [PDF]
Heliyon, 2023 Liu Y +6 more
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State-wide increase in prenatal diagnosis of klinefelter syndrome on amniocentesis and chorionic villus sampling: Impact of non-invasive prenatal testing for sex chromosome conditions. [PDF]
Prenat Diagn, 2023 Loughry L +4 more
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Conditions Mimicking the Cancer Microenvironment Modulate the Functional Outcome of Human Chorionic Villus Mesenchymal Stem/Stromal Cells in vitro. [PDF]
Front Cell Dev Biol, 2021 Basmaeil Y +3 more
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Uniparental Disomy and Genome Imprinting: an Overview [PDF]
, 2017 The following paper is concerned with potential changes in the normal epigenetic process in a diploid individual, when a chromosome pair or segment is inherited from one parent only, instead of the expected biparental contribution.
Engel, E.
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Prenatal Diagnostic Procedures.
Journal of Health Science and Medical Research (JHSMR), 2010 Prenatal invasive procedures serve two purposes-diagnostic and therapeutic. In diagnostic tests, the aim is to identify structural or functional abnormalities of the embryo or fetus in utero.
Tharangrat Hanprasertpong
doaj
Chorionic villus-derived mesenchymal stem cell-mediated autophagy promotes the proliferation and invasiveness of trophoblasts under hypoxia by activating the JAK2/STAT3 signalling pathway. [PDF]
Cell Biosci, 2021 Chu Y +13 more
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Detection of Cryptic Fragile X Full Mutation Alleles by Southern Blot in a Female and Her Foetal DNA via Chorionic Villus Sampling, Complicated by Mosaicism for 45,X0/46,XX/47,XXX. [PDF]
Genes (Basel), 2021 Pandelache A +7 more
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New approach for estimating risk of miscarriage after chorionic villus sampling. [PDF]
Ultrasound Obstet Gynecol, 2020 Gil MM +15 more
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Costs and Benefits of Prenatal Screening For Cystic Fibrosis [PDF]
Newly-developed genetic tests based on restriction fragment length polymorphisms (RFLPs) promise to facilitate the early detection of genetic diseases. Several such tests are now available for the prenatal detection of cystic fibrosis (CF), a common and ...
Alan M. Garber, Joseph P. Fenerty
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