Subject
Clinical Biochemistry,General Medicine
Reference5 articles.
1. Steroid 21-hydroxylase deficiency: two additional mutations in salt-wasting disease and rapid screening of disease-causing mutations;Wedell;Hum Mol Genet,1993
2. Genotyping is a valuable diagnostic complement to neonatal screening for congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency;Nordenstrom;J Clin Endocrinol Metab,1999
3. Disease expression and molecular genotype in congenital adrenal hyperplasia due to 21-hydroxylase deficiency;Speiser;J Clin Invest,1992
4. Mutational spectrum of the steroid 21-hydroxylase gene in Sweden: implications for genetic diagnosis and association with disease manifestation;Wedell;J Clin Endocrinol Metab,1994
5. Predicting phenotype in steroid 21-hydroxylase deficiency? Comprehensive genotyping in 155 unrelated, well defined patients from Southern Germany;Krone;J Clin Endocrinol Metab,2000
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