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Citation: Ojc. Hellwinkel et al., A unique exonic splicing mutation in the human androgen receptor gene indicates a physiologic relevance of regular androgen receptor transcript variants, J CLIN END, 86(6), 2001, pp. 2569-2575

Authors: Hellwinkel, OJC Bull, K Holterhus, PM Homburg, N Struve, D Hiort, O

Citation: Ojc. Hellwinkel et al., Complete androgen insensitivity caused by a splice donor site mutation in intron 2 of the human androgen receptor gene resulting in an exon 2-lackingtranscript with premature stop-codon and reduced expression, J STEROID B, 68(1-2), 1999, pp. 1-9

Authors: Holterhus, PM Sinnecker, GHG Wollmann, HA Struve, D Homburg, N Kruse, K Hiort, O

Citation: Pm. Holterhus et al., Expression of two functionally different androgen receptors in a patient with androgen insensitivity, EUR J PED, 158(9), 1999, pp. 702-706