A multiplex PCR amplicon sequencing assay to screen genetic hearing loss variants in newborns

Location
Deutsche Nationalbibliothek Frankfurt am Main
ISSN
1755-8794
Extent
Online-Ressource
Language
Englisch
Notes
online resource.

Bibliographic citation
A multiplex PCR amplicon sequencing assay to screen genetic hearing loss variants in newborns ; volume:14 ; number:1 ; day:27 ; month:2 ; year:2021 ; pages:1-8 ; date:12.2021
BMC medical genomics ; 14, Heft 1 (27.2.2021), 1-8, 12.2021

Creator
Yang, Haiyan
Luo, Hongyu
Zhang, Guiwei
Zhang, Junqing
Peng, Zhiyu
Xiang, Jiale
Contributor
SpringerLink (Online service)

DOI
10.1186/s12920-021-00906-1
URN
urn:nbn:de:101:1-2021041514500510142080
Rights
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Last update
14.08.2025, 10:45 AM CEST

Data provider

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Associated

  • Yang, Haiyan
  • Luo, Hongyu
  • Zhang, Guiwei
  • Zhang, Junqing
  • Peng, Zhiyu
  • Xiang, Jiale
  • SpringerLink (Online service)

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