Matches in Nanopublications for { ?s ?p "[Primary pigmented nodular adrenocortical disease (PPNAD) and pituitary adenoma in a boy with sporadic Carney complex due to a novel, de novo paternal PRKAR1A mutation (R96X).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP870284.RAmO_NeJwYa_QG-Sgd5hZ9aw5Z9H_vydc3L9yxoKJeDMs130_assertion description "[Primary pigmented nodular adrenocortical disease (PPNAD) and pituitary adenoma in a boy with sporadic Carney complex due to a novel, de novo paternal PRKAR1A mutation (R96X).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP870284.RAmO_NeJwYa_QG-Sgd5hZ9aw5Z9H_vydc3L9yxoKJeDMs130_provenance.
- NP642260.RAc1GHNQeU6U5T7KBEZiAfsdv3XZR-RoqnD08dVnMasNw130_assertion description "[Primary pigmented nodular adrenocortical disease (PPNAD) and pituitary adenoma in a boy with sporadic Carney complex due to a novel, de novo paternal PRKAR1A mutation (R96X).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP642260.RAc1GHNQeU6U5T7KBEZiAfsdv3XZR-RoqnD08dVnMasNw130_provenance.
- assertion description "[Primary pigmented nodular adrenocortical disease (PPNAD) and pituitary adenoma in a boy with sporadic Carney complex due to a novel, de novo paternal PRKAR1A mutation (R96X).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP601939.RAIqAq66jpnEFeF_3k5Mf1uZlc5IJqSHPbYJ1yldUAjCQ130_assertion description "[Primary pigmented nodular adrenocortical disease (PPNAD) and pituitary adenoma in a boy with sporadic Carney complex due to a novel, de novo paternal PRKAR1A mutation (R96X).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP601939.RAIqAq66jpnEFeF_3k5Mf1uZlc5IJqSHPbYJ1yldUAjCQ130_provenance.
- NP601938.RA8BkxJiC6s7mPvx2lbXcHj4lW91EDI8eLKR-lGxtnRtE130_assertion description "[Primary pigmented nodular adrenocortical disease (PPNAD) and pituitary adenoma in a boy with sporadic Carney complex due to a novel, de novo paternal PRKAR1A mutation (R96X).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP601938.RA8BkxJiC6s7mPvx2lbXcHj4lW91EDI8eLKR-lGxtnRtE130_provenance.