Shallow whole genome sequencing is well suited for the detection of chromosomal aberrations in human blastocysts

詳細情報 詳細情報について

• CRID

  1360574093500489088

• DOI

  10.1016/j.fertnstert.2015.07.1144

• ISSN

  00150282

• Web Site

  https://api.elsevier.com/content/article/PII:S0015028215016556?httpAccept=text/plain

  https://api.elsevier.com/content/article/PII:S0015028215016556?httpAccept=text/xml

• データソース種別

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