Authors:
THILEN A
NORDENSTROM A
HAGENFELDT L
VONDOBELN U
GUTHENBERG C
LARSSON A
Citation: A. Thilen et al., BENEFITS OF NEONATAL SCREENING FOR CONGENITAL ADRENAL-HYPERPLASIA (21-HYDROXYLASE DEFICIENCY) IN SWEDEN, Pediatrics, 101(4), 1998, pp. 111-115
Authors:
THILEN A
WOODS KA
PERRY LA
SAVAGE MO
WEDELL A
RITZEN EM
Citation: A. Thilen et al., EARLY GROWTH IS NOT INCREASED IN UNTREATED MODERATELY SEVERE 21-HYDROXYLASE DEFICIENCY, Acta paediatrica, 84(8), 1995, pp. 894-898
Authors:
WEDELL A
THILEN A
RITZEN EM
STENGLER B
LUTHMAN H
Citation: A. Wedell et al., MUTATIONAL SPECTRUM OF THE STEROID 21-HYDROXYLASE GENE IN SWEDEN - IMPLICATIONS FOR GENETIC DIAGNOSIS AND ASSOCIATION WITH DISEASE MANIFESTATION, The Journal of clinical endocrinology and metabolism, 78(5), 1994, pp. 1145-1152