A clinical survey of mosaic single nucleotide variants in disease-causing genes detected by exome sequencing
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1756-994X
- Umfang
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Online-Ressource
- Sprache
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Englisch
- Anmerkungen
-
online resource.
- Erschienen in
-
A clinical survey of mosaic single nucleotide variants in disease-causing genes detected by exome sequencing ; volume:11 ; number:1 ; day:26 ; month:7 ; year:2019 ; pages:1-11 ; date:12.2019
Genome medicine ; 11, Heft 1 (26.7.2019), 1-11, 12.2019
- Urheber
-
Cao, Ye
Tokita, Mari J.
Chen, Edward S.
Ghosh, Rajarshi
Chen, Tiansheng
Feng, Yanming
Gorman, Elizabeth
Gibellini, Federica
Ward, Patricia A.
Braxton, Alicia
Wang, Xia
Meng, Linyan
Xiao, Rui
Bi, Weimin
Xia, Fan
Eng, Christine M.
Yang, Yaping
Gambin, Tomasz
Shaw, Chad
Liu, Pengfei
Stankiewicz, Pawel
- Beteiligte Personen und Organisationen
-
SpringerLink (Online service)
- DOI
-
10.1186/s13073-019-0658-2
- URN
-
urn:nbn:de:101:1-2019121901183509793000
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
14.08.2025, 10:54 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
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Beteiligte
- Cao, Ye
- Tokita, Mari J.
- Chen, Edward S.
- Ghosh, Rajarshi
- Chen, Tiansheng
- Feng, Yanming
- Gorman, Elizabeth
- Gibellini, Federica
- Ward, Patricia A.
- Braxton, Alicia
- Wang, Xia
- Meng, Linyan
- Xiao, Rui
- Bi, Weimin
- Xia, Fan
- Eng, Christine M.
- Yang, Yaping
- Gambin, Tomasz
- Shaw, Chad
- Liu, Pengfei
- Stankiewicz, Pawel
- SpringerLink (Online service)
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