S.M. Baumgartner-Parzer
Department of Internal Medicine III
Division of Endocrinology and Metabolism
Waehringer Guertel 18-20
A-1090 Vienna
Austria
Name/email consistency: high
- Predisposition for de novo gene aberrations in the offspring of mothers with a duplicated CYP21A2 gene. Baumgartner-Parzer, S.M., Fischer, G., Vierhapper, H. J. Clin. Endocrinol. Metab. (2007)
- Carrier frequency of congenital adrenal hyperplasia (21-hydroxylase deficiency) in a middle European population. Baumgartner-Parzer, S.M., Nowotny, P., Heinze, G., Waldhäusl, W., Vierhapper, H. J. Clin. Endocrinol. Metab. (2005)
- Polymorphisms in exon 13 and intron 14 of the RET protooncogene: genetic modifiers of medullary thyroid carcinoma?. Baumgartner-Parzer, S.M., Lang, R., Wagner, L., Heinze, G., Niederle, B., Kaserer, K., Waldhäusl, W., Vierhapper, H. J. Clin. Endocrinol. Metab. (2005)