Genotype–Phenotype Correlation in Children With Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency Using Next Generation Sequencing June 2025 in “ Molecular Genetics & Genomic Medicine ” Nurgül Ataş, Murat Karaoğlan, Gülper Nacarkahya We don't know much about this study yet. We're maintaining the world's largest resposity of hair loss research. You can help out the community by sending a PDF of this study here . Not sure how to get a study's PDF? You can email the authors of the study. View this study on onlinelibrary.wiley.com →
research EMQN Best Practice Guidelines for Molecular Genetic Testing and Reporting of 21-Hydroxylase Deficiency 94 citations , July 2020 in “European Journal of Human Genetics” The guidelines ensure accurate genetic testing and reporting for 21-hydroxylase deficiency.