Procedure for neonatal screening for congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Donaldson, M. et al. (2001) Procedure for neonatal screening for congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Hormone Research, 55, pp. 201-205.

Full text not currently available from Enlighten.


Item Type:Articles
Status:Published
Refereed:Yes
Glasgow Author(s) Enlighten ID:Donaldson, Dr Malcolm
Authors: Donaldson, M., Ferrandez-Longas, A., Giovanelli, G., Grueters-Kieslich, A., Hnikova, O., Honour, J., Klett, M., Larsson, A., Schrama, S., Torresani, T., and Toublanc, J.
College/School:College of Medical Veterinary and Life Sciences > School of Medicine, Dentistry & Nursing > Clinical Specialities
Journal Name:Hormone Research

University Staff: Request a correction | Enlighten Editors: Update this record