1 results
21ohd genetics pathophysiology peds
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... also known as "congenital ... a scrotum #21HydroxylaseDeficiency ... pathophysiology #genetics #endocrinology ... #peds #pediatrics
No results found for "Pediatric Tracheostomy Algorithm pediatrics congenital headtrauma clinical endocrinology video 21hydroxylasedeficiency"
Try removing search terms or sorting by relevance
Or Upload an image for you and others searching for #Pediatric #Tracheostomy #Algorithm #pediatrics #congenital #headtrauma #clinical #endocrinology #video #21hydroxylasedeficiency