Diagnosis of classical steroid 21-hydroxylase deficiency using an HLA-B locus-specific DNA-probe
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference28 articles.
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1. Prenatal diagnosis of 21-hydroxylase deficiency caused by gene conversion and rearrangements: pitfalls and molecular diagnostic solutions;Prenatal Diagnosis;2002
2. An Overview of Molecular Diagnosis of Steroid 21-Hydroxylase Deficiency;The Journal of Molecular Diagnostics;2001-05
3. Single-Nucleotide Polymorphisms in Intron 2 of CYP21P: Evidence for a Higher Rate of Mutation at CpG Dinucleotides in the Functional Steroid 21-Hydroxylase Gene and Application to Segregation Analysis in Congenital Adrenal Hyperplasia;Clinical Chemistry;1999-05-01
4. Characterization of frequent polymorphisms in intron 2 of CYP21: application to analysis of segregation of CYP21 alleles;Clinical Chemistry;1998-12-01
5. Analysis of four common salt-wasting mutations in CYP21 (steroid 21-hydroxylase) by cleavase fragment length polymorphism analysis and characterization of a frequent polymorphism in intron 6;Molecular Diagnosis;1998-09
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