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Article

Confirmation of mosaicism and uniparental disomy in amniocytes, after detection of mosaic chromosome abnormalities in chorionic villi

18 Jan 2006

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Share to Genetic Syndromes and Imprinting
Share to Genomic variations and chromosomal abnormalities
Share to Prenatal Screening and Diagnostics

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 16418738
DOI: 10.1038/sj.ejhg.5201564

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Related research

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Confirmation of mosaicism and uniparental disomy in amniocytes, after detection of mosaic chromosome abnormalities in chorionic villiPMID 16418738Read ↗

Revised guidelines for the diagnosis of mosaicism in amniocytesSemantic proximity Read ↗

Interpreting mosaicism in chorionic villi: results of a monocentric series of 1001 mosaics in chorionic villi with follow-up amniocentesisSemantic proximity Read ↗

Failure of prenatal diagnosis of diploid–triploid mosaicism after amniocentesisSemantic proximity Read ↗

True fetal mosaicism revealed by a single abnormal colony in amniocyte cultureSemantic proximity Read ↗

Mosaicism and uniparental disomy in prenatal diagnosisSemantic proximity Read ↗

Mosaic trisomy 2 at amniocentesis: Prenatal diagnosis and molecular genetic analysisSemantic proximity Read ↗

Determining chorionicity and amnionicity in twin pregnancies: PitfallsSemantic proximity Read ↗

Prenatally detected trisomy 20 mosaicismSemantic proximity Read ↗

(Potential) false-negative diagnoses in chorionic villi and a review of the literatureSemantic proximity Read ↗

Chorionic villus sampling and amniocentesisSemantic proximity Read ↗

Reevaluating confined placental mosaicismSemantic proximity Read ↗

Origin of amnion and implications for evaluation of the fetal genotype in cases of mosaicism.Semantic proximity Read ↗

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