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Article

Shallow whole genome sequencing is well suited for the detection of chromosomal aberrations in human blastocysts

14 Aug 2015

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Share to Genetic Syndromes and Imprinting
Share to Genomic variations and chromosomal abnormalities
Share to Prenatal Screening and Diagnostics

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 26282994
DOI: 10.1016/j.fertnstert.2015.07.1144

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