William Dobyns to Primary Myelofibrosis
This is a "connection" page, showing publications William Dobyns has written about Primary Myelofibrosis.
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Expanding the SHOC2 mutation associated phenotype of Noonan syndrome with loose anagen hair: structural brain anomalies and myelofibrosis. Am J Med Genet A. 2013 Oct; 161A(10):2420-30.
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