Matches in Nanopublications for { ?s ?p "[Background/Aims: Mutations in the HESX1 gene are associated with a broad spectrum of phenotypes: septo-optic dysplasia, midline defects, pituitary abnormalities with consequent hypopituitarism, isolated growth hormone (GH) deficiency or combined pituitary hormone deficiencies (CPHD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 2 of
2
with 100 items per page.
- NP540182.RAshuMCdSOlJxHCZ3WNpvY-DJC8KzjHUnYkvK3-PVCqiw130_assertion description "[Background/Aims: Mutations in the HESX1 gene are associated with a broad spectrum of phenotypes: septo-optic dysplasia, midline defects, pituitary abnormalities with consequent hypopituitarism, isolated growth hormone (GH) deficiency or combined pituitary hormone deficiencies (CPHD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP540182.RAshuMCdSOlJxHCZ3WNpvY-DJC8KzjHUnYkvK3-PVCqiw130_provenance.
- NP727089.RA4s7d_y2ayIq4SHTgpR42hX7PQlFnqRRvrd1tIZrEYDg130_assertion description "[Background/Aims: Mutations in the HESX1 gene are associated with a broad spectrum of phenotypes: septo-optic dysplasia, midline defects, pituitary abnormalities with consequent hypopituitarism, isolated growth hormone (GH) deficiency or combined pituitary hormone deficiencies (CPHD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP727089.RA4s7d_y2ayIq4SHTgpR42hX7PQlFnqRRvrd1tIZrEYDg130_provenance.