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