Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Search Results
3 results
Filters applied: . Clear all
Results are displayed in a computed author sort order.
The Publication Date timeline is not available.
Page 1
Novel GLI2 mutations identified in patients with Combined Pituitary Hormone Deficiency (CPHD): Evidence for a pathogenic effect by functional characterization.
Clin Endocrinol (Oxf). 2019 Mar;90(3):449-456. doi: 10.1111/cen.13914. Epub 2019 Jan 7.
Clin Endocrinol (Oxf). 2019.
PMID: 30548673
Variations in the high-mobility group-A2 gene (HMGA2) are associated with idiopathic short stature.
Fusco I, Babu D, Mellone S, Barizzone N, Prodam F, Fanelli A, Muniswamy R, Petri A, Bellone S, Bona G, Giordano M.
Fusco I, et al. Among authors: muniswamy r.
Pediatr Res. 2016 Feb;79(2):258-61. doi: 10.1038/pr.2015.225. Epub 2015 Nov 4.
Pediatr Res. 2016.
PMID: 26536448
Item in Clipboard
Frequency of genetic defects in combined pituitary hormone deficiency: a systematic review and analysis of a multicentre Italian cohort.
De Rienzo F, Mellone S, Bellone S, Babu D, Fusco I, Prodam F, Petri A, Muniswamy R, De Luca F, Salerno M, Momigliano-Richardi P, Bona G, Giordano M; Italian Study Group on Genetics of CPHD.
De Rienzo F, et al. Among authors: muniswamy r.
Clin Endocrinol (Oxf). 2015 Dec;83(6):849-60. doi: 10.1111/cen.12849. Epub 2015 Aug 6.
Clin Endocrinol (Oxf). 2015.
PMID: 26147833
Review.
Item in Clipboard
Cite
Cite
ARTICLE TYPE
ARTICLE LANGUAGE
AGE
Filters on the sidebar will be reset to the default list and any currently applied filters will be cleared.