CYP21A2 mutation update: Comprehensive analysis of databases and published genetic variants - Simonetti - 2018 - Human Mutation - Wiley Online Library
Different possible forms of the RCCX region and CYP21A2 gene. (a)... | Download Scientific Diagram
Approximate location of the CYP21A2 gene mutations | Download Scientific Diagram
Clinical and biochemical description of a novel CYP21A2 gene mutation 962_963insA using a new 3D model for the P450c21 protein in: European Journal of Endocrinology Volume 155 Issue 1 (2006)
Schematic representation of the mechanism of gene conversion, where a... | Download Scientific Diagram
CYP21A2 Gene - GeneCards | CP21A Protein | CP21A Antibody
The chimeric CYP21P/CYP21 gene and 21-hydroxylase deficiency | Journal of Human Genetics
Functional Studies of p.R132C, p.R149C, p.M283V, p.E431K, and a Novel c.652-2A>G Mutations of the CYP21A2 Gene | PLOS ONE
The CYP21A2 gene and its duplicated pseudogene (CYP21A1P). a Both genes... | Download Scientific Diagram
Mapping of a de novo unequal crossover causing a deletion of the steroid 21-hydroxylase (CYP21A2) gene and a non-functional hybrid tenascin-X (TNXB) gene | Journal of Medical Genetics
Distribution of the most common mutations along the CYP21A2 gene that... | Download Scientific Diagram
C4B null alleles are not associated with genetic polymorphisms in the adjacent gene CYP21A2in autism | BMC Medical Genetics | Full Text
Identification of a novel compound heterozygous mutation of the CYP21A2 gene causing 21‑hydroxylase deficiency in a Chinese pedigree
Genotype–phenotype correlation in 1,507 families with congenital adrenal hyperplasia owing to 21-hydroxylase deficiency | PNAS
Frontiers | Molecular Diagnosis of Steroid 21-Hydroxylase Deficiency: A Practical Approach
Location of the PCR primers used to detect the mutations in CYP21A2 gene | Download Scientific Diagram
Figure 3 from Molecular genetics of 21-hydroxylase deficiency. | Semantic Scholar
A previously undescribed mutation detected by sequence analysis of CYP21A2 gene in an infant with salt wasting congenital adrenal hyperplasia
CYP21A2 Gene - GeneCards | CP21A Protein | CP21A Antibody
![PDF] Intraspecific Evolution of Human RCCX Copy Number Variation Traced by Haplotypes of the CYP21A2 Gene | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/b880d42126bf1060754ebf0040265f54bd68a760/3-Figure1-1.png "PDF] Intraspecific Evolution of Human RCCX Copy Number Variation Traced by Haplotypes of the CYP21A2 Gene | Semantic Scholar")
PDF] Intraspecific Evolution of Human RCCX Copy Number Variation Traced by Haplotypes of the CYP21A2 Gene | Semantic Scholar
EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency | European Journal of Human Genetics
Implications of <i>CYP21A2</i> gene duplications in carrier screening and prenatal diagnosis of congenital adrenal hyperplasia due to 21 Hydroxylase deficiency
Frontiers | Genes and Pseudogenes: Complexity of the RCCX Locus and Disease
Identification of a novel compound heterozygous mutation of the CYP21A2 gene causing 21‑hydroxylase deficiency in a Chinese pedigree
2+0 CYP21A2 deletion carrier — a limitation of the genetic testing and counseling: A case report
Common mutations in the CYP21A2 gene. The schematic indicates the... | Download Scientific Diagram
