The search for the genetic contribution to autoimmune thyroid disease: the never ending story?
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Title
The search for the genetic contribution to autoimmune thyroid disease: the never ending story?
Authors
Keywords
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Journal
Briefings in Functional Genomics
Volume 10, Issue 2, Pages 77-90
Publisher
Oxford University Press (OUP)
Online
2011-05-05
DOI
10.1093/bfgp/elq036
References
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- (2010) Nadir R. Farid et al. TISSUE ANTIGENS
- The HapMap and Genome-Wide Association Studies in Diagnosis and Therapy
- (2009) Teri A. Manolio et al. Annual Review of Medicine
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- DNA variations in human and medical genetics: 25 years of my experience
- (2009) Yusuke Nakamura JOURNAL OF HUMAN GENETICS
- Finding the missing heritability of complex diseases
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- (2008) Thomas A. Pearson JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION
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