Confined placental mosaicism for trisomies 2, 3, 7, 8, 9, 16, and 22: their incidence, likely origins, and mechanisms for cell lineage compartmentalization
about
Clinical aspects, prenatal diagnosis, and pathogenesis of trisomy 16 mosaicismMeiotic origin of trisomy in confined placental mosaicism is correlated with presence of fetal uniparental disomy, high levels of trisomy in trophoblast, and increased risk of fetal intrauterine growth restrictionFalse Negative NIPT Results: Risk Figures for Chromosomes 13, 18 and 21 Based on Chorionic Villi Results in 5967 Cases and Literature ReviewEuropean collaborative research on mosaicism in CVS (EUCROMIC)--fetal and extrafetal cell lineages in 192 gestations with CVS mosaicism involving single autosomal trisomyConfined placental mosaicism for trisomy 8 and intra-uterine growth retardation.Mosaic inv dup(8p) marker chromosome with stable neocentromere suggests neocentromerization is a post-zygotic event.Trisomy 7 mosaicism, maternal uniparental heterodisomy 7 and Hirschsprung's disease in a child with Silver-Russell syndrome.Factors controlling embryo viability.Somatic genome variations in health and diseaseSomatic genomic variations in early human prenatal development.Developmental ability of chromosomally abnormal human embryos to develop to the blastocyst stage.Chromosomal Mosaicism in Human Feto-Placental Development: Implications for Prenatal Diagnosis.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.Different probe combinations for assessment of postzygotic chromosomal imbalances in human embryos.Chromosomal microarray versus karyotyping for prenatal diagnosis.Evaluation of triploid<-->diploid and trisomy-3<-->diploid mouse chimeras as models for investigating how lineage restriction occurs in confined placental mosaicism.Mosaic aneuploidy in early fetal losses.Rare autosomal trisomies, revealed by maternal plasma DNA sequencing, suggest increased risk of feto-placental disease.Cytogenetic confirmation of a positive NIPT result: evidence-based choice between chorionic villus sampling and amniocentesis depending on chromosome aberration.Should we 'open the kimono' to release the results of rare autosomal aneuploidies following noninvasive prenatal whole genome sequencing?Genome-wide cfDNA screening: clinical laboratory experience with the first 10,000 cases.Trisomy 8 in pediatric acute myeloid leukemia: A NOPHO-AML study.Confirmation of mosaicism and uniparental disomy in amniocytes, after detection of mosaic chromosome abnormalities in chorionic villi.Inverted duplications: how many of them are mosaic?A second case of intrauterine growth retardation and primary hypospadias associated with a trisomy 22 placenta but with biparental inheritance of chromosome 22 in the fetus.Paternal isodisomy for chromosome 2 as the cause of Crigler-Najjar type I syndrome.Comprehensive molecular cytogenetic analysis of the human blastocyst stage.Origin and clinical relevance of chromosomal aberrations other than the common trisomies detected by genome-wide NIPS: results of the TRIDENT study.Trisomy 3 confined placental mosaicism: a management dilemma.Cytogenetic analysis of spontaneous abortions: comparison of techniques and assessment of the incidence of confined placental mosaicism.Partial trisomy 3p and partial monosomy 11q associated with atrial septal defect, cleft palate, and developmental delay: a case report.Evidence for high frequency of chromosomal mosaicism in spontaneous abortions revealed by interphase FISH analysis.Maternal uniparental heterodisomy for chromosome 2: detection through 'atypical' maternal AFP/hCG levels, with an update on a previous case.Confined placental mosaicism revisited: Impact on pregnancy characteristics and outcome.Structural chromosomal abnormalities detected during CVS analysis and their role in the prenatal ascertainment of cryptic subtelomeric rearrangementsTwo cases of placental T21 mosaicism: challenging the detection limits of non-invasive prenatal testingAssessing the role of placental trisomy in preeclampsia and intrauterine growth restriction
P2860
Q24678124-E50FB0BE-FB1D-4083-96F8-114223508DEFQ24680385-8B3FE60F-4CD6-48CF-92BF-33C7BEA641BCQ26771694-416E9BAD-016A-41B2-8F7A-FE569B086BA7Q28236672-E39150AF-FCB8-43ED-9E23-7CECBC8E361FQ30472943-E5DE0D19-FF56-4CF1-A604-BBCA580C6BE8Q34084979-4AFCF20A-C69C-49C6-A3F0-28D76D247E8DQ34421272-BF1FE0BD-C361-4344-98D0-E4663F33F0BCQ34446776-3C440E2A-E87B-4522-B6B8-DADD9FB64754Q34479594-88AD5441-473D-4787-BC89-C0D9BC620710Q34479598-3F32BA11-9203-457B-BA2E-0ECA6897DABEQ34517295-622B58E5-7E46-4AE6-80E5-2E4B46B5B5A1Q35667141-85581B77-338E-4780-88C3-03EE4A24A679Q35786166-8EB82A78-37AB-4E8F-8E3E-774A02FC53C8Q36271289-C0786DDF-E853-4A0C-86AD-6319AB8ECCF6Q36546668-2B8F0DDE-E1CC-44B8-9188-956F81949872Q37372453-CDC35935-D6FF-4DC9-A9F0-8B8EE8173CF7Q37839567-07B6F04D-0537-469F-8675-7257BEF1AE0EQ38601652-6BF5ECA7-00CE-4904-BE20-24187D92F403Q38728695-00484A4E-7612-4436-9C0A-D375B4D157B8Q39068479-9A23D3F5-0919-42F0-93C1-445A92134100Q39375461-61FFCEB7-8F3F-432D-9C4A-8FCFC5C49496Q39788816-28A7DD23-839A-4995-976E-49047EA73817Q40328374-1A5ECD17-F782-4435-8A40-5709355F3FAEQ40533026-B590B033-B74D-4CFC-B0A1-2DDAA7881196Q40749209-6B153005-6D16-452E-94C0-19FD000F8938Q45178769-875324D4-409A-4086-A087-18084962E3B5Q48743163-A0665CAB-C5DD-4F96-AC21-57D67F4F2F51Q50093623-93B1B8BA-FE0C-41F6-B534-FD980EE80157Q50559352-EBA59BB8-594B-4A06-8C0A-2AF5E9D90242Q50929865-DA84014E-7FAA-428B-AF5D-26367255E15CQ51864752-50847013-70F0-43A3-AC60-18DDC9ADD53CQ51932472-C665CD84-0705-45E1-9B86-55FD2DF19356Q51961478-AA5F561B-D12F-4CF4-A0D6-E300051F4668Q52591806-6B8B0101-FB16-4CD2-9781-A603D1507D14Q56977193-B7125DE6-3520-46DF-A6EF-FD42FC8352E3Q57097369-D2881949-1F9D-4560-B1E0-0F3AA448157EQ58623881-D929FBB7-20FD-4629-B222-4822422A7044
P2860
Confined placental mosaicism for trisomies 2, 3, 7, 8, 9, 16, and 22: their incidence, likely origins, and mechanisms for cell lineage compartmentalization
description
1996 nî lūn-bûn
@nan
1996 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
1996 թվականի հունիսին հրատարակված գիտական հոդված
@hy
1996年の論文
@ja
1996年論文
@yue
1996年論文
@zh-hant
1996年論文
@zh-hk
1996年論文
@zh-mo
1996年論文
@zh-tw
1996年论文
@wuu
name
Confined placental mosaicism f ...... l lineage compartmentalization
@ast
Confined placental mosaicism f ...... l lineage compartmentalization
@en
Confined placental mosaicism f ...... l lineage compartmentalization
@nl
type
label
Confined placental mosaicism f ...... l lineage compartmentalization
@ast
Confined placental mosaicism f ...... l lineage compartmentalization
@en
Confined placental mosaicism f ...... l lineage compartmentalization
@nl
prefLabel
Confined placental mosaicism f ...... l lineage compartmentalization
@ast
Confined placental mosaicism f ...... l lineage compartmentalization
@en
Confined placental mosaicism f ...... l lineage compartmentalization
@nl
P2860
P1433
P1476
Confined placental mosaicism f ...... l lineage compartmentalization
@en
P2093
J Wolstenholme
P2860
P304
P356
10.1002/(SICI)1097-0223(199606)16:6<511::AID-PD904>3.0.CO;2-8
P407
P577
1996-06-01T00:00:00Z