2 results
pediatrics peds 21hydroxylasedeficiency 21ohd praderwilli syndrome
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Syndrome Signs/Symptoms ... /Complications: ... fractures • Short ... PraderWilli #Syndrome #genetics ... #pathophysiology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology
No results found for "sports pathophysiology pocus symptoms complications coronavirus lupus genetics endocrinology"
Try removing search terms or sorting by relevance
Or Upload an image for you and others searching for #sports #pathophysiology #pocus #symptoms #complications #coronavirus #lupus #genetics #endocrinology