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Q34107765-0892A410-955A-4071-857B-20988C2E39CC
Q34107765-0892A410-955A-4071-857B-20988C2E39CC
BestRank
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http://www.wikidata.org/entity/statement/Q34107765-0892A410-955A-4071-857B-20988C2E39CC
Discovery of common sequences absent in the human reference genome using pooled samples from next generation sequencing.
P2860
Q34107765-0892A410-955A-4071-857B-20988C2E39CC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34107765-0892A410-955A-4071-857B-20988C2E39CC
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dc7fe73043b455f83738dab11264d8244bf21fba
P2860
Estimates of the frequency of chromosome abnormalities detectable in unselected newborns using moderate levels of banding