1 results
21hydroxylasedeficiency 21ohd pediatrics peds
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology
No results found for "Morisons rush causes pathophysiology signs rheumatology symptoms endocrinology comparison genetics"
Try removing search terms or sorting by relevance
Or Upload an image for you and others searching for #Morisons #rush #causes #pathophysiology #signs #rheumatology #symptoms #endocrinology #comparison #genetics