1 results
21ohd endocrinology genetics pediatrics peds
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... enzyme 21-OHase causes ... Signs/Symptoms/Complications ... a scrotum #21HydroxylaseDeficiency ... #21OHD #pathophysiology
No results found for "Maturation iron pathophysiology clinical complications orthopedics disease msk causes 21hydroxylasedeficiency"
Try removing search terms or sorting by relevance
Or Upload an image for you and others searching for #Maturation #iron #pathophysiology #clinical #complications #orthopedics #disease #msk #causes #21hydroxylasedeficiency