Pathogenesis of chromosomal mosaicism and its effect on early human development

scientific article (publication date: 6 March 2000)

Pathogenesis of chromosomal mosaicism and its effect on early human development is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1002/(SICI)1096-8628(20000306)91:1<39::AID-AJMG7>3.0.CO;2-L
P698PubMed publication ID10751087

P2093author name stringD K Kalousek
P2860cites workMolecular cytogenetic detection of confined gonadal mosaicism in a conceptus with trisomy 16 placental mosaicismQ24539906
Confined placental mosaicism, IUGR, and adverse pregnancy outcome: a controlled retrospective U.K. collaborative surveyQ28248049
Origin of extraembryonic mesoderm in experimental animals: relevance to chorionic mosaicism in humansQ28260141
Chromosomal mosaicism confined to the placenta in human conceptionsQ28275224
Pallister-Killian syndrome: cytogenetic and molecular studiesQ28283068
Comparative genomic hybridization for molecular cytogenetic analysis of solid tumorsQ29618818
Implantation and the placenta: key pieces of the development puzzleQ33367178
Quantitative analysis of comparative genomic hybridizationQ38509783
Transgenes as molecular probes for genomic imprinting.Q39579376
Prenatal aneuploidy detection in interphase cells by fluorescence in situ hybridization (FISH).Q40448517
An audit of trisomy 16 in man.Q40546787
Mosaic trisomy 16 ascertained through amniocentesis: evaluation of 11 new casesQ40982708
A chimaeric animal model for confined placental mosaicismQ41034149
Trisomy 7 CVS mosaicism: pregnancy outcome, placental and DNA analysis in 14 casesQ41151687
The primordial germ cells of mammals: some current perspectivesQ41486520
A male with trisomy 9 mosaicism and maternal uniparental disomy for chromosome 9 in the euploid cell lineQ41599996
Manufactured hexaparental mice show that adults are derived from three embyronic cellsQ45020809
United States survey on chromosome mosaicism and pseudomosaicism in prenatal diagnosisQ45153294
Is non-isotopic in situ hybridization finally coming of age?Q59060550
Cell Selection in vivo in Normal/G Trisomic MosaicsQ59087268
P433issue1
P407language of work or nameEnglishQ1860
P921main subjectpathogenesisQ372016
P304page(s)39-45
P577publication date2000-03-06
P1433published inAmerican Journal of Medical Genetics Part AQ15755121
P1476titlePathogenesis of chromosomal mosaicism and its effect on early human development
P478volume91

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cites work (P2860)
Q46893392Analysis of human invasive cytotrophoblasts using multicolor fluorescence in situ hybridization
Q46032152Aneuploidy involving chromosome 1 in failed-fertilized human oocytes is unrelated to maternal age.
Q37543845Aneuploidy: from a physiological mechanism of variance to Down syndrome
Q34636041Array comparative genomic hybridization analyses of all blastomeres of a cohort of embryos from young IVF patients revealed significant contribution of mitotic errors to embryo mosaicism at the cleavage stage
Q36186418Bioinformatic Tools Identify Chromosome-Specific DNA Probes and Facilitate Risk Assessment by Detecting Aneusomies in Extra-embryonic Tissues
Q40783786Cell-cycle kinetics of cell lines from patients with chromosomal mosaicism
Q35667141Chromosomal Mosaicism in Human Feto-Placental Development: Implications for Prenatal Diagnosis
Q40159257Chromosomal anomalies in early spontaneous abortions: interphase FISH analysis on 855 FFPE first trimester abortions
Q38641797Chromosomal instability in mammalian pre-implantation embryos: potential causes, detection methods, and clinical consequences
Q37327116Chromosomal mosaicism in mouse two-cell embryos after paternal exposure to acrylamide
Q34276317Chromosome segregation defects contribute to aneuploidy in normal neural progenitor cells.
Q36589856Chromosome-specific DNA repeats: rapid identification in silico and validation using fluorescence in situ hybridization
Q40328374Confirmation of mosaicism and uniparental disomy in amniocytes, after detection of mosaic chromosome abnormalities in chorionic villi.
Q34399858Constitutional aneuploidy in the normal human brain.
Q37212268DNA probe pooling for rapid delineation of chromosomal breakpoints
Q38947803Genetics of the human placenta: implications for toxicokinetics.
Q59615335High Performance DNA Probes for Perinatal Detection of Numerical Chromosome Aberrations
Q46064223Human cytotrophoblasts acquire aneuploidies as they differentiate to an invasive phenotype
Q53091843Implications of fetoplacental mosaicism on cell-free DNA testing: a review of a common biological phenomenon.
Q36873757Inducing segmental aneuploid mosaicism in the mouse through targeted asymmetric sister chromatid event of recombination
Q52871460Massively Parallel Sequencing (MPS) of Cell-Free Fetal DNA (cffDNA) for Trisomies 21, 18, and 13 in Twin Pregnancies.
Q52164101Maternal uniparental disomy of chromosome 16 and body stalk anomaly.
Q35135033Mechanisms of mosaicism, chimerism and uniparental disomy identified by single nucleotide polymorphism array analysis
Q46318081Microarray analysis reveals abnormal chromosomal complements in over 70% of 14 normally developing human embryos.
Q37839567Mosaic aneuploidy in early fetal losses.
Q28198469Mutation of the doublecortin gene in male patients with double cortex syndrome: somatic mosaicism detected by hair root analysis
Q43442678Premature ovarian failure due to tetrasomy X in an adolescent girl
Q37751386Prenatal diagnosis and genetic counseling for mosaic trisomy 13.
Q34550372Rapid mapping of chromosomal breakpoints: from blood to BAC in 20 days
Q34479604Somatic genomic variations in extra-embryonic tissues
Q57636633The role of morphology in combination with ploidy analysis in characterizing early gestational abortion
Q53553989The unprecedented recurrent diploid/tetraploid mosaicism of trisomy-18 (mixoploidy; 4n+18/2n+18): clinical report.

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