Detection of ≥1 Mb microdeletions and microduplications in a single cell using custom oligonucleotide arrays

ABSTRACT Objective High resolution detection of genomic copy number abnormalities in a single cell is relevant to preimplantation genetic diagnosis and potentially to noninvasive prenatal diagnosis. Our objective is to develop a reliable array comparative genomic hybridization (CGH) platform to dete...

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Veröffentlicht in:	Prenatal diagnosis 2012-01, Vol.32 (1), p.10-20
Hauptverfasser:	Bi, Weimin, Breman, Amy, Shaw, Chad A., Stankiewicz, Pawel, Gambin, Tomasz, Lu, Xinyan, Cheung, Sau Wai, Jackson, Laird G., Lupski, James R., den Veyver, Ignatia B. Van, Beaudet, Arthur L.
Format:	Artikel
Sprache:	eng
Online-Zugang:	Volltext
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