1 results
21hydroxylasedeficiency endocrinology genetics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Females may be labeled ... Signs/Symptoms/Complications ... #pathophysiology ... endocrinology #peds ... #pediatrics
No results found for "SIDS peds video sign labeled pyramidal pediatrics 21ohd abcs pathophysiology"
Try removing search terms or sorting by relevance
Or Upload an image for you and others searching for #SIDS #peds #video #sign #labeled #pyramidal #pediatrics #21ohd #abcs #pathophysiology