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Results: 4

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: RITZEN EM THILEN A WOODS KA PERRY LA SAVAGE MO WEDELL A
Citation: Em. Ritzen et al., ARE INFANTS INSENSITIVE TO ANDROGEN - COMMENTS, Acta paediatrica, 85(6), 1996, pp. 761-761

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
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