Suchergebnisse - "Liu, Qin"

PubPharm (13)

1

Author Correction : Conservation of copy number profiles during engraftment and passaging of patient-derived cancer xenografts

enthalten in: Nature genetics | 2021

von Woo, X. | Giordano, J. | Srivastava, A. | +161

ErratumFor: Nat Genet. 2021 Jan;53(1):86-99. - PMID 33414553

2

Conservation of copy number profiles during engraftment and passaging of patient-derived cancer xenografts

enthalten in: Nature genetics | 2021

von Woo, X. | Giordano, J. | Srivastava, A. | +161

ErratumIn: Nat Genet. 2021 May;53(5):761. - PMID 33608693

3

Corrigendum: Genome-wide association study of esophageal squamous cell carcinoma in Chinese subjects identifies susceptibility loci at PLCE1 and C20orf54

enthalten in: Nature genetics | 2014

von Wang, L. | Zhou, F. | Li, X. | +96

4

NMNAT1 mutations cause Leber congenital amaurosis

enthalten in: Nature genetics | 2012

von Falk, M. | Zhang, Q. | Nakamaru-Ogiso, E. | +26

CommentIn: Clin Genet. 2013 Jan;83(1):33-4. - PMID 23088368

5

NMNAT1 mutations cause Leber congenital amaurosis

enthalten in: Nature genetics | 2012

von Falk, M. | Zhang, Q. | Nakamaru-Ogiso, E. | +26

6

Corrigendum: TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum

enthalten in: Nature genetics | 2011

von Davis, E. | Zhang, Q. | Liu, Q. | +44

7

TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum

enthalten in: Nature genetics | 2011

von Davis, E. | Zhang, Q. | Liu, Q. | +44

8

TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum

enthalten in: Nature genetics | 2011

von Davis, E. | Zhang, Q. | Liu, Q. | +45

9

TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum

enthalten in: Nature genetics | 23 January 2011

von Davis, E. | Zhang, Q. | Liu, Q. | +44

10

Candidate exome capture identifies mutation of SDCCAG8 as the cause of a retinal-renal ciliopathy

enthalten in: Nature genetics | 2010

von Otto, E. | Hurd, T. | Airik, R. | +52

CommentIn: Clin Genet. 2011 Mar;79(3):222-4. - PMID 21199495