Matches in Nanopublications for { ?s ?p "[Mutations in the GHRH receptor (GHRHR) gene (GHRHR) cause autosomal recessive isolated GH deficiency (IGHD), and are usually associated with anterior pituitary hypoplasia (APH) (defined as pituitary height more than 2 SDS below normal).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP344415.RArCiQL_Wl36mzIF_d2Eb-jWeAkw0wciCTTEINzVIKM2Y130_assertion description "[Mutations in the GHRH receptor (GHRHR) gene (GHRHR) cause autosomal recessive isolated GH deficiency (IGHD), and are usually associated with anterior pituitary hypoplasia (APH) (defined as pituitary height more than 2 SDS below normal).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP344415.RArCiQL_Wl36mzIF_d2Eb-jWeAkw0wciCTTEINzVIKM2Y130_provenance.
- NP532954.RAqgnF9pTF4jRl5-OtJaYZCXrcFirFZcd5tbU5OINMJpw130_assertion description "[Mutations in the GHRH receptor (GHRHR) gene (GHRHR) cause autosomal recessive isolated GH deficiency (IGHD), and are usually associated with anterior pituitary hypoplasia (APH) (defined as pituitary height more than 2 SDS below normal).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP532954.RAqgnF9pTF4jRl5-OtJaYZCXrcFirFZcd5tbU5OINMJpw130_provenance.
- NP188675.RAEmfZ7BXGGDv-QHjSBP-BqoipcH-_Txkbj4sKtAYlasg130_assertion description "[Mutations in the GHRH receptor (GHRHR) gene (GHRHR) cause autosomal recessive isolated GH deficiency (IGHD), and are usually associated with anterior pituitary hypoplasia (APH) (defined as pituitary height more than 2 SDS below normal).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188675.RAEmfZ7BXGGDv-QHjSBP-BqoipcH-_Txkbj4sKtAYlasg130_provenance.