High-resolution melting curve (HRM) analysis to establish CYP21A2 mutations converted from the CYP21A1P in congenital adrenal hyperplasia
Author:
Publisher
Elsevier BV
Subject
Biochemistry, medical,Clinical Biochemistry,Biochemistry,General Medicine
Reference42 articles.
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1. Phenotype heterogeneity of congenital adrenal hyperplasia due to genetic mosaicism and concomitant nephrogenic diabetes insipidus in a sibling;BMC Medical Genetics;2018-07-11
2. Rapid Identification of FGFR2 Gene Mutations in Taiwanese Patients With Endometrial Cancer Using High-resolution Melting Analysis;Applied Immunohistochemistry & Molecular Morphology;2015-08
3. Direct assessment of cytochrome P450 2D6 genotypes by high-resolution melting analysis and DNA sequencing;Environmental Toxicology and Pharmacology;2014-11
4. Molecular Genetics of 21‐Hydroxylase Deficiency;eLS;2014-09-15
5. Novel method to characterize CYP21A2 in Florida patients with congenital adrenal hyperplasia and commercially available cell lines;Molecular Genetics and Metabolism Reports;2014
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