Mosaic trisomy 15 at amniocentesis: Prenatal diagnosis, molecular genetic analysis and literature review (Q26783419)

7

Wayseen Wang

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Schu-Rern Chern

2

Schu-Rern Chern

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Chih-Ping Chen

1

Chih-Ping Chen

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Chien-Wen Yang

5

Chien-Wen Yang

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author name string

Yen-Ni Chen

3

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Li-Feng Chen

Taiwanese Journal of Obstetrics & Gynecology

6

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language of work or name

English

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publication date

August 2015

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published in

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Third Prader-Willi syndrome phenotype due to maternal uniparental disomy 15 with mosaic trisomy 15

PubMed

volume

54

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issue

4

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page(s)

426-31

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cites work

1 reference

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Uniparental disomy (UPD) other than 15: phenotypes and bibliography updated.

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Mosaic trisomy 15 in a liveborn infant

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Trisomy 15 mosaicism owing to familial reciprocal translocation t(1;15): implication for prenatal diagnosis.

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Prenatal diagnosis, fetal pathology and cytogenetic analysis of a 46,XX/47,XX, + 15 mosaic

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A Canadian collaborative study of mosaicism in amniotic fluid cell cultures

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Mosaic trisomy 15 found at amniocentesis

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True trisomy 15 mosaicism, detected by amniocentesis at 12 weeks of gestation and fetal echocardiography

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Trisomy 15 mosaicism and uniparental disomy (UPD) in a liveborn infant

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Trisomy 15 mosaic derived from trisomic conceptus: report of a case and a review

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Delineation of a clinical syndrome caused by mosaic trisomy 15

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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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Low-level mosaicism for both trisomy 15 and monosomy-X in amniotic fluid cells confirmed in fetal tissues

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Prenatal testing for uniparental disomy: indications and clinical relevance

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Mosaic trisomy 12 at amniocentesis: prenatal diagnosis and molecular genetic analysis

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Discrepancy in the trisomy mosaicism level between cultured amniocytes and uncultured amniocytes in prenatally detected mosaic trisomy 20.

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Application of interphase FISH to uncultured amniocytes for rapid confirmation of true trisomy 2 mosaicism in the case of suspected amniocyte mosaicism involving trisomy 2 in a single colony

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Prenatal diagnosis of mosaic trisomy 2 associated with abnormal maternal serum screening, oligohydramnios, intrauterine growth restriction, ventricular septal defect, preaxial polydactyly, and facial dysmorphism

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Prenatal diagnosis of mosaic trisomy 12 associated with congenital overgrowth

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Interphase FISH on uncultured amniocytes at repeat amniocentesis for rapid diagnosis of true mosaicism in a case of level II mosaicism involving trisomy 21 in a single colony from an in situ culture of amniocytes

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Trisomy 15 associated with nonimmune hydrops

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Mosaic trisomy 15 in a short girl with hemihypotrophy and mental retardation.

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An infant with trisomy 15 mosaicism

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Prenatal diagnosis of low level trisomy 15 mosaicism: review of the literature

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A case of trisomy of chromosome 15

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Prader-Willi syndrome in a child with mosaic trisomy 15 and mosaic triplo-X: a molecular analysis

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7 January 2021