Erratum to: Genome-wide copy number variation association study suggested VPS13B gene for osteoporosis in Caucasians

Author： Deng F.-Y.   Zhao L.-J.   Pei Y.-F.   Sha B.-Y.   Liu X.-G.   Yan H.   Wang L.   Yang T.-L.   Recker R.   Papasian C.   Deng H.-W.  

Publisher： Springer Publishing Company

ISSN： 0937-941X

Source： Osteoporosis International, Vol.21, Iss.8, 2010-08, pp. : 1455-1455

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Related content

Rapid Diagnosis of Imprinting Disorders Involving Copy Number Variation and Uniparental Disomy Using Genome-Wide SNP Microarrays

By  

Cytogenetic and Genome Research, Vol. 146, Iss. 1, 2015-07 ,pp. : 9-18

Karger

Access to resources Recommend Favorite

Copy number variation in the genome; the human DMD gene as an example

By  

Cytogenetic and Genome Research, Vol. 115, Iss. 3-4, 2006-11 ,pp. : 240-246

Karger

Access to resources Recommend Favorite

Genome-Wide Mapping Of Copy Number Variations using SNP Arrays

By  

Transfusion Medicine and Hemotherapy, Vol. 36, Iss. 4, 2009-07 ,pp. : 246-251

Karger

Access to resources Recommend Favorite

Pooling-Based Genome-Wide Association Study Implicates Gamma-Glutamyltransferase 1 (GGT1) Gene in Pancreatic Carcinogenesis

By  

Pancreatology, Vol. 10, Iss. 2-3, 2010-05 ,pp. : 194-200

Karger

Access to resources Recommend Favorite

Brief Report: Genome‐Wide Association Study Identifies ITPR2 as a Susceptibility Gene for Kashin‐Beck Disease in Han Chinese

By  

ARTHRITIS & RHEUMATOLOGY, Vol. 67, Iss. 1, 2015-01 ,pp. : 176-181

John Wiley & Sons Inc

Access to resources Recommend Favorite