A Novel GHR Intronic Variant, c.266+83G>T, Activates a Cryptic 5′ Splice Site Causing Severe GHR Deficiency and Classical GH Insensitivity Syndrome von Feigerlova, Eva, Swinyard, Mike, Derr, Michael A., Farnsworth, Jeannie, Andrew, Shayne F., Rosenfeld, Ron G., Hwa, Vivian

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