换一批Preface. Use of genome-wide oligonucleotide- or SNP-array platforms has widened the spectrum of detectable human genomic variation.
第一作者：
Poot M
作者：
关键词
DNA Copy Number VariationsGenetic DiseasesInborn*Genetic VariationGenomeHuman*Genome-Wide Association StudyHumans*Oligonucleotide Array Sequence Analysis*PolymorphismSingle NucleotideReview Literature as TopicISSN Electronic1424-859XISSN Linking1424-8581Publication TypeIntroductory Journal Article.LanguageEnglishElectronic Date of Publication20111203Date Created20111213
发布时间
2013-11-20
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