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Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|September 10, 2005
Mutations in the amino-terminal domain of the human androgen receptor may be associated with partial androgen insensitivity and impaired transactivation in vitroP-M Holterhus, R Werner, D Struve, et al.
The Journal of Steroid Biochemistry and Molecular Biology|April 24, 1999
Complete androgen insensitivity caused by a splice donor site mutation in intron 2 of the human androgen receptor gene resulting in an exon 2-lacking transcript with premature stop-codon and reduced expressionO J Hellwinkel, K Bull, P M Holterhus, et al.
The Journal of Clinical Endocrinology and Metabolism|June 9, 2001
A unique exonic splicing mutation in the human androgen receptor gene indicates a physiologic relevance of regular androgen receptor transcript variantsO J Hellwinkel, P M Holterhus, D Struve, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|January 26, 2006
Mobile diabetes education and care: intervention for children and young people with Type 1 diabetes in rural areas of northern GermanyS von Sengbusch, E Müller-Godeffroy, S Häger, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|March 12, 2009
Mutation analysis of FOXF2 in patients with disorders of sex development (DSD) in combination with cleft palateU Jochumsen, R Werner, N Miura, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|April 9, 2008
Altered transcription profiles of key-enzymes of androgen biosynthesis in genital skin fibroblasts from patients with 46,XY disorders of sex development (DSD)U Hoppe, L Wünsch, P-M Holterhus, et al.
Human Reproduction (Oxford, England)|November 26, 1999
Genetics of male subfertility: consequences for the clinical work-upW Küpker, E Schwinger, O Hiort, et al.
Hormone Research|August 31, 2000
Clinical, endocrine, and molecular genetic findings in patients with 17beta-hydroxysteroid dehydrogenase deficiencyW Twesten, P Holterhus, W G Sippell, et al.
The Journal of Pediatrics|November 5, 1997
Etiologic classification of severe hypospadias: implications for prognosis and managementN Albers, C Ulrichs, S Glüer, et al.
European Journal of Pediatrics|June 1, 1996
Molecular genetic analysis and human chorionic gonadotropin stimulation tests in the diagnosis of prepubertal patients with partial 5 alpha-reductase deficiencyO Hiort, H Willenbring, N Albers, et al.
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