Barely Significant
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A germline mutation of CDKN2A and a novel RPLP1-C19MC fusion detected in a rare melanotic neuroectodermal tumor of infancy: a case report.

BMC Cancer · 2016 · PMC4983003 · PMID 27519597

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a slight trendno p-value reported
There is a slight trend towards a greater incidence in males than females (ratio = 1.48) [ 1 ].

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