Braun, Andreas

Predicting phenotype in steroid 21-hydroxylase deficiency? Comprehensive genotyping in 155 unrelated, well defined patients from southern Germany

Krone, N., Braun, A., Roscher, A. A., Knorr, D., & Schwarz, H. P. (2000) · The Journal of Clinical Endocrinology & Metabolism

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 397

Molecular analysis of the gene for the human vitamin-D-binding protein (group-specific component): allelic differences of the common genetic GC types

Braun, A., Bichlmaier, R., & Cleve, H. (1992) · Human Genetics

Vitamin D Research StudiesGenetic Associations and Epidemiology

Cited by 137

Symptoms in carriers of adrenoleukodystrophy relate to skewed X inactivation

Maier, E. M., Kammerer, S., Muntau, A. C., Wichers, M., Braun, A., & Roscher, A. A. (2002) · Annals of Neurology

Metabolism and Genetic DisordersGenetics and Neurodevelopmental Disorders

Cited by 72

Association of X-Linked Adrenoleukodystrophy with HLA DRB1 Alleles

Berger, J., Bernheimer, H., Fae, I., Braun, A., Roscher, A., Molzer, B., & Fischer, G. (1995) · Biochemical and Biophysical Research Communications

Metabolism and Genetic DisordersLysosomal Storage Disorders Research

Cited by 16