Mosaic trisomy 2 at amniocentesis: prenatal diagnosis and molecular genetic analysis (Q26830630)

Yu-Ting Chen

series ordinal

4

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Jun-Wei Su

series ordinal

6

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Chen-Wen Pan

series ordinal

7

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language of work or name

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December 2012

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Taiwanese Journal of Obstetrics & Gynecology

published in

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volume

51

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issue

4

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page(s)

603-11

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Maternal uniparental disomy of chromosome 2 in a baby with trisomy 2 mosaicism in amniotic fluid culture

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True trisomy 2 mosaicism in amniocytes and newborn liver associated with multiple system abnormalities

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Confined placental mosaicism for trisomies 2, 3, 7, 8, 9, 16, and 22: their incidence, likely origins, and mechanisms for cell lineage compartmentalization

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Maternal uniparental disomy for chromosome 2 in association with confined placental mosaicism for trisomy 2 and severe intrauterine growth retardation

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Trisomy 2: confined placental mosaicism in a fetus with intrauterine growth retardation

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Rare trisomy mosaicism diagnosed in amniocytes, involving an autosome other than chromosomes 13, 18, 20, and 21: karyotype/phenotype correlations

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Accuracy of cytogenetic findings on chorionic villus sampling (CVS)--diagnostic consequences of CVS mosaicism and non-mosaic discrepancy in centres contributing to EUCROMIC 1986-1992

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Prenatal diagnosis of mosaic trisomy 2: discrepancy between molecular cytogenetic analyses of uncultured amniocytes and karyotyping of cultured amniocytes in a pregnancy with severe fetal intrauterine growth restriction

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Prenatal diagnosis of mosaic trisomy 8: Clinical report and literature review

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Mosaic trisomy 9 at amniocentesis: prenatal diagnosis and molecular genetic analyses

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

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A trisomy 2 fetus with severe neural tube defects and other abnormalities

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The phenotypic spectrum of trisomy 2: report of two new cases

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A case of mosaic trisomy 2 diagnosed at amniocentesis in an abnormal fetus and confirmed in multiple fetal tissues

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Prenatal diagnosis of trisomy 2 mosaicism: a case report

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