(Q28290041)

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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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Europe PubMed Central

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

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author name string

J Wolstenholme

1

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language of work or name

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publication date

June 1996

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Prenatal Diagnosis

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16

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6

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511-24

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Double autosomal/gonosomal mosaic aneuploidy: study of nondisjunction in two cases with trisomy of chromosome 8.

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Follow-up of pregnancies complicated by placental mosaicism diagnosed by chorionic villus sampling

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Current assessment of fetal losses as a direct consequence of chorionic villus sampling

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Restricted distribution of tetraploid cells in mouse tetraploid<==>diploid chimaeras.

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Anatomic and chromosomal anomalies in 639 spontaneous abortuses

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Genomic imprinting related to prenatal diagnosis

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Spontaneous abortion and confined chromosomal mosaicism

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Confined placental mosaicism in CVS and pregnancy outcome.

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Prenatal diagnosis of trisomy 9. Six cases and a review of the literature

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Molecular cytogenetic analysis of term placentae suspected of mosaicism using fluorescence in situ hybridization

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Confined placental mosaicism

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The European collaborative study on mosaicism in chorionic villus sampling: data from 1986 to 1987.

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Chorionic villi sampling: laboratory experience with 4,000 consecutive cases

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A case of paternal uniparental disomy for chromosome 11.

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An audit of trisomy 16 in man.

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Confined placental mosaicism, IUGR, and adverse pregnancy outcome: a controlled retrospective U.K. collaborative survey

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21 January 2018

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10.1002/(SICI)1097-0223(199606)16:6<511::AID-PD904>3.0.CO;2-8

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