A prospective evaluation of whole-exome sequencing as a first-tier molecular test in infants with suspected monogenic disorders

Details 詳細情報について

• CRID

  1360857597844744960

• DOI

  10.1038/gim.2016.1

• ISSN

  10983600

• Web Site

  http://www.nature.com/articles/gim20161.pdf

  http://www.nature.com/articles/gim20161

  https://api.elsevier.com/content/article/PII:S1098360021013903?httpAccept=text/xml

  https://api.elsevier.com/content/article/PII:S1098360021013903?httpAccept=text/plain

  http://www.nature.com/doifinder/10.1038/gim.2016.1

• Data Source

  • Crossref