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Showing page 1 of results 1 - 1 of about 1 matches for "jullian-e"

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Genotype/phenotype correlation of PRKAR1A mutations in patients with Carney complex (CNC) and/or sporadic primary pigmented nodular adrenocortical disease (PPNAD) from the CNC network
L Groussin; F Rene-Corail; L Cazabat; E Jullian; E Clauser; X Bertagna; J Bertherat
Published: 2006-12-04

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