Rare Diseases
Records 1 - 2 (of 2 Records) |
Query Trace: 21-hydroxylase Deficiency[original query]>>Guidelines Related[Product Type] |
---|
EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency. Baumgartner-Parzer Sabina et al. European journal of human genetics : EJHG 2020 Jul |
Guidelines for diagnosis and treatment of 21-hydroxylase deficiency (2014 revision). et al. Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology 2015 Jul 24(3) 77-105 |