Showing results (21-30 of 28) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 28 results.
American Journal of Medical Genetics. Part A|May 6, 2016
An emerging, recognizable facial phenotype in association with mutations in GLI-similar 3 (GLIS3)Paul Dimitri, Elisa De Franco, Abdelhadi M Habeb, et al.
Archives of Disease in Childhood|June 1, 1993
Neurological and adrenal dysfunction in the adrenal insufficiency/alacrima/achalasia (3A) syndromeD B Grant, N D Barnes, M Dumic, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|August 30, 2002
Serum leptin and leptin binding activity in children and adolescents with hypothalamic dysfunctionL Patel, C D Cooper, N D Quinton, et al.
The Journal of Clinical Endocrinology and Metabolism|August 11, 2015
Expanding the Clinical Spectrum Associated With GLIS3 MutationsP Dimitri, A M Habeb, F Gurbuz, et al.
The Journal of Clinical Investigation|March 28, 2017
Somatic mutations and progressive monosomy modify SAMD9-related phenotypes in humansFederica Buonocore, Peter Kühnen, Jenifer P Suntharalingham, et al.
The New England Journal of Medicine|April 30, 2004
Activating mutations in the gene encoding the ATP-sensitive potassium-channel subunit Kir6.2 and permanent neonatal diabetesAnna L Gloyn, Ewan R Pearson, Jennifer F Antcliff, et al.
Pageof 3