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Article

Long term follow‐up of developmental delay in a child with prenatally‐diagnosed trisomy 20 mosaicism

8 Jul 2005

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Share to Genomic variations and chromosomal abnormalities
Share to Pediatric Hepatobiliary Diseases and Treatments
Share to Prenatal Screening and Diagnostics

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 16007609
DOI: 10.1002/ajmg.a.30825

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Long term follow‐up of developmental delay in a child with prenatally‐diagnosed trisomy 20 mosaicismPMID 16007609Read ↗

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Prenatally detected trisomy 20 mosaicismSemantic proximity Read ↗

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Non-mosaic trisomy 20 of paternal origin in chorionic villus and amniotic fluid also detected in fetal blood and other tissuesSemantic proximity Read ↗

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