Browsing bySubjectcopy number variation

Jump to:
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
  • Sort by:
  • In order:
  • Results/Page
  • Authors/Record:

Showing results 1 to 2 of 2

Issue DateTitleAuthor(s)Type
2021Expectations and blind spots for structural variation detection from long-read assemblies and short-read genome sequencing technologiesCharles LeeArticle
2016One CNV Discordance in NRXN1 Observed Upon Genome-wide Screening in 38 Pairs of Adult Healthy Monozygotic Twins이동환Article

BROWSE