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  • Search Condition : Filter (MeSH = Human Growth Hormone / deficiency*)
Species Resource Title
Human and Animal Cells COS-1(RCB0143) A novel and de novo splice-donor site mutation in intron 3 of the GH-1 gene in a patient with isolated growth hormone deficiency.
Human and Animal Cells COS-7(RCB0539) , 293T(RCB2202) Adult combined GH, prolactin, and TSH deficiency associated with circulating PIT-1 antibody in humans.