Common variants at 10p12.31, 10q21.1 and 13q12.13 are associated with sporadic pituitary adenoma

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WAVE3 is associated with invasiveness in prostate cancer cells

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Profound, prelingual nonsyndromic deafness maps to chromosome 10q21 and is caused by a novel missense mutation in the Usher syndrome type IF gene PCDH15

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Wnt Pathway Inhibitors Are Strongly Down-Regulated in Pituitary Tumors

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