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Q28256361-9679F155-4031-4F26-B41D-7BC4662DF559
Q28256361-9679F155-4031-4F26-B41D-7BC4662DF559
BestRank
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http://www.wikidata.org/entity/statement/Q28256361-9679F155-4031-4F26-B41D-7BC4662DF559
A copy number variation map of the human genome
P2860
Q28256361-9679F155-4031-4F26-B41D-7BC4662DF559
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28256361-9679F155-4031-4F26-B41D-7BC4662DF559
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58b0ca6d2dfc681d2ef4fcea82b35c0942948e57
P2860
Estimates of the frequency of chromosome abnormalities detectable in unselected newborns using moderate levels of banding