Pages that link to "Q24678681"
Jump to navigation
Jump to search
The following pages link to Beckwith-Wiedemann syndrome and assisted reproduction technology (ART) (Q24678681):
Displaying 50 items.
- In vitro fertilization may increase the risk of Beckwith-Wiedemann syndrome related to the abnormal imprinting of the KCN1OT gene (Q24532045) (← links)
- Beckwith-Wiedemann syndrome and IVF: a case-control study (Q24533595) (← links)
- Genomic imprinting disorders in humans: a mini-review (Q24646016) (← links)
- Comparative isoschizomer profiling of cytosine methylation: the HELP assay (Q24685607) (← links)
- Correlation of sperm penetration assay score with polyspermy rate in in-vitro fertilization (Q24792615) (← links)
- New advances of preimplantation and prenatal genetic screening and noninvasive testing as a potential predictor of health status of babies (Q26822531) (← links)
- Dysmorphology demystified (Q28298817) (← links)
- The history of cancer epigenetics (Q29617273) (← links)
- Peri-implantation hormonal milieu: elucidating mechanisms of abnormal placentation and fetal growth (Q30408297) (← links)
- Skewed X inactivation and IVF-conceived infants (Q30435048) (← links)
- Child health, developmental plasticity, and epigenetic programming (Q30466805) (← links)
- The primate embryo gene expression resource: a novel resource to facilitate rapid analysis of gene expression patterns in non-human primate oocytes and preimplantation stage embryos (Q30827441) (← links)
- Cdkn1c (p57Kip2) is the major regulator of embryonic growth within its imprinted domain on mouse distal chromosome 7. (Q33285306) (← links)
- Assisted Reproductive Technology affects developmental kinetics, H19 Imprinting Control Region methylation and H19 gene expression in individual mouse embryos (Q33303250) (← links)
- Immature cryopreserved ovary restores puberty and fertility in mice without alteration of epigenetic marks (Q33328492) (← links)
- Germline mutation in NLRP2 (NALP2) in a familial imprinting disorder (Beckwith-Wiedemann Syndrome). (Q33419813) (← links)
- In vitro fertilization and embryo culture strongly impact the placental transcriptome in the mouse model (Q33532631) (← links)
- DNA methylation patterns in tissues from mid-gestation bovine foetuses produced by somatic cell nuclear transfer show subtle abnormalities in nuclear reprogramming (Q33537490) (← links)
- Effects of ooplasm manipulation on DNA methylation and growth of progeny in mice (Q33586272) (← links)
- Epigenetics in the placenta (Q33620204) (← links)
- Sperm DNA damage in male infertility: etiologies, assays, and outcomes (Q33679414) (← links)
- Infant leukemia and parental infertility or its treatment: a Children's Oncology Group report (Q33862981) (← links)
- Epigenetics and assisted reproductive technology: a call for investigation (Q33909693) (← links)
- The impact of assisted reproductive technologies on genomic imprinting and imprinting disorders (Q34011361) (← links)
- Effects of assisted reproduction technology on placental imprinted gene expression (Q34035548) (← links)
- Addition of H19 'loss of methylation testing' for Beckwith-Wiedemann syndrome (BWS) increases the diagnostic yield. (Q34084829) (← links)
- Making the blastocyst: lessons from the mouse (Q34108232) (← links)
- Similar DNA methylation levels in specific imprinting control regions in children conceived with and without assisted reproductive technology: a cross-sectional study (Q34203901) (← links)
- Rare congenital disorders, imprinted genes, and assisted reproductive technology (Q34205147) (← links)
- Imprinting methylation errors in ART. (Q34277727) (← links)
- Low frequency of imprinting defects in ICSI children born small for gestational age. (Q34325361) (← links)
- Specific epigenetic alterations of IGF2-H19 locus in spermatozoa from infertile men (Q34328467) (← links)
- Association between Beckwith-Wiedemann syndrome and assisted reproductive technology: a case series of 19 patients. (Q34393122) (← links)
- Bringing epigenetics into the diagnostics of the andrology laboratory: challenges and perspectives (Q34433307) (← links)
- Familial molar tissues due to mutations in the inflammatory gene, NALP7, have normal postzygotic DNA methylation (Q34552072) (← links)
- Genetic or epigenetic difference causing discordance between monozygotic twins as a clue to molecular basis of mental disorders (Q34556925) (← links)
- Outcome of assisted reproduction. (Q34581482) (← links)
- A review of known imprinting syndromes and their association with assisted reproduction technologies. (Q34595528) (← links)
- A survey of assisted reproductive technology births and imprinting disorders. (Q34699309) (← links)
- Maternal and zygotic Dnmt1 are necessary and sufficient for the maintenance of DNA methylation imprints during preimplantation development (Q34786920) (← links)
- Imprinting disorders and assisted reproductive technology (Q34845922) (← links)
- Sperm DNA damage: clinical significance in the era of assisted reproduction (Q34998961) (← links)
- Methodology matters: IVF versus ICSI and embryonic gene expression (Q35151072) (← links)
- Scientific hazards of human reproductive 'cloning'. (Q35180365) (← links)
- A potential use of embryonic stem cell medium for the in vitro culture of preimplantation embryos (Q35205842) (← links)
- The periconceptional environment and cardiovascular disease: does in vitro embryo culture and transfer influence cardiovascular development and health? (Q35227826) (← links)
- Analysis of H19 methylation in control and abnormal human embryos, sperm and oocytes (Q35406359) (← links)
- Increased prevalence of imprinting defects in patients with Angelman syndrome born to subfertile couples (Q35448168) (← links)
- DNA methylation differences between in vitro- and in vivo-conceived children are associated with ART procedures rather than infertility (Q35504751) (← links)
- Is intracytoplasmic sperm injection safe? (Q35558541) (← links)