P W Speiser

Detection of steroid 21-hydroxylase alleles using gene-specific PCR and a multiplexed ligation detection reaction.

F. Barany, P. White, P. Speiser, 1995, Genomics.

Identification of non-amplifying CYP21 genes when using PCR-based diagnosis of 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH) affected pedigrees.

F. Barany, P. White, P. Speiser, 1996, Human molecular genetics.

Insulin insensitivity in adrenal hyperplasia due to nonclassical steroid 21-hydroxylase deficiency.

M. New, P. Speiser, J. Serrat, 1992, The Journal of clinical endocrinology and metabolism.