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Dajiang J. Liu et al.
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Valgerdur Steinthorsdottir et al.
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Or Zuk et al.
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Andy Boyd et al.
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Hong-Shan Wei et al.
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Megan L. Grove et al.
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zCall: a rare variant caller for array-based genotyping
Jacqueline I. Goldstein et al.
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Julius Gudmundsson et al.
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Jian Yang et al.
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Evolution and Functional Impact of Rare Coding Variation from Deep Sequencing of Human Exomes
Jacob A. Tennessen et al.
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Matthew B. Lanktree et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2011)
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Michael C. Wu et al.
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Genomic inflation factors under polygenic inheritance
Jian Yang et al.
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Cristen J. Willer et al.
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Claus Gyrup et al.
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Brendan J. Frey et al.
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NA Sims et al.
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Secreted antagonists of the Wnt signalling pathway
Y Kawano et al.
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Y Takeuchi et al.
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Chondrodysplasias due to proteoglycan defects
NB Schwartz et al.
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Molecular cloning and biological activity of a novel lysyl oxidase-related gene expressed in cartilage
H Ito et al.
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Expression of recombinant human pregnancy-associated plasma protein-A and identification of the proform of eosinophil major basic protein as its physiological inhibitor
MT Overgaard et al.
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