1 results
21hydroxylasedeficiency pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... , vomiting • Late ... #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
No results found for "late pathophysiology difficult peds clinical symptoms differential endocrinology genetics 21ohd"
Try removing search terms or sorting by relevance
Or Upload an image for you and others searching for #late #pathophysiology #difficult #peds #clinical #symptoms #differential #endocrinology #genetics #21ohd