A novel mutation in STK11 gene is associated with Peutz-Jeghers Syndrome in Chinese patients
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1471-2350
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
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A novel mutation in STK11 gene is associated with Peutz-Jeghers Syndrome in Chinese patients ; volume:12 ; number:1 ; day:14 ; month:12 ; year:2011 ; pages:1-5 ; date:12.2011
BMC medical genetics ; 12, Heft 1 (14.12.2011), 1-5, 12.2011
- Creator
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Wang, Zhiqing
- Contributor
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Chen, Yulan
Wu, Baoping
Zheng, Haoxuan
He, Jiman
Jiang, Bo
SpringerLink (Online service)
- DOI
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10.1186/1471-2350-12-161
- URN
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urn:nbn:de:1111-2016071513840
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 10:48 AM CEST
Data provider
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Associated
- Wang, Zhiqing
- Chen, Yulan
- Wu, Baoping
- Zheng, Haoxuan
- He, Jiman
- Jiang, Bo
- SpringerLink (Online service)
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