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Increased nuchal translucency with normal karyotype: a follow‐up study of 100 cases supplemented with CGH and MLPA analyses

1 Dec 2009

Abstract excerpt

OBJECTIVE: To evaluate whether high-resolution comparative genomic hybridization (HR-CGH) and subtelomeric and syndrome-specific multiplex ligation-dependent probe amplification (MLPA) would detect minor chromosomal aberrations in fetuses with increased nuchal translucency thickness (NT) and normal karyotype on conventional karyotyping. METHODS: Chorionic villus samples from 100 fetuses with NT > or = 99(th)...

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PMID: 19953565
DOI: 10.1002/uog.7468

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