Genes, pseudogenes and like genes: The case of 21-hydroxylase in Italian population - ScienceDirect
The CYP21A2 gene and its duplicated pseudogene (CYP21A1P). a Both genes... | Download Scientific Diagram
Frontiers | Molecular Diagnosis of Steroid 21-Hydroxylase Deficiency: A Practical Approach
Frontiers | The pathogenic p.Gln319Ter variant is not causing congenital adrenal hyperplasia when inherited in one of the duplicated CYP21A2 genes
EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency | European Journal of Human Genetics
Genotype–phenotype correlation in 1,507 families with congenital adrenal hyperplasia owing to 21-hydroxylase deficiency | PNAS
Genotyping of CYP21A2 for Congenital Adrenal Hyperplasia Screening using Allele-Specific Primer Extension followed by Bead Array Hybridization | SpringerLink
Identification of a novel compound heterozygous mutation of the CYP21A2 gene causing 21‑hydroxylase deficiency in a Chinese pedigree
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
Frontiers | The Complexities in Genotyping of Congenital Adrenal Hyperplasia: 21-Hydroxylase Deficiency
Defining The RCCX Phenotype – Metabolic Healing
JCM | Free Full-Text | Comprehensive Genetic Testing of CYP21A2: A Retrospective Analysis in Patients with Suspected Congenital Adrenal Hyperplasia
Salt-wasting congenital adrenal hyperplasia phenotype as a result of the TNXA/TNXB chimera 1 (CAH-X CH-1) and the pathogenic IVS2-13A/C > G in CYP21A2 gene | Hormones
Common mutations in the CYP21A2 gene. The schematic indicates the... | Download Scientific Diagram
Novel variants of CYP21A2 in Vietnamese patients with congenital adrenal hyperplasia - Chi - 2019 - Molecular Genetics & Genomic Medicine - Wiley Online Library
2+0 CYP21A2 deletion carrier — a limitation of the genetic testing and counseling: A case report
CYP21A2 Gene - GeneCards | CP21A Protein | CP21A Antibody
C4B null alleles are not associated with genetic polymorphisms in the adjacent gene CYP21A2in autism | BMC Medical Genetics | Full Text
Frontiers | The Complexities in Genotyping of Congenital Adrenal Hyperplasia: 21-Hydroxylase Deficiency
IJMS | Free Full-Text | In Silico Structural and Biochemical Functional Analysis of a Novel CYP21A2 Pathogenic Variant
Overcoming high homology to detect variation in CYP21A2 with whole-genome sequencing in DRAGEN
Different possible forms of the RCCX region and CYP21A2 gene. (a)... | Download Scientific Diagram
A new CYP21A1P/CYP21A2chimeric gene identified in an Italian woman suffering from classical congenital adrenal hyperplasia form | BMC Medical Genetics | Full Text
![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
Novel method to characterize CYP21A2 in Florida patients with congenital adrenal hyperplasia and commercially available cell lines - ScienceDirect
CYP21A2 mutation update: Comprehensive analysis of databases and published genetic variants - Simonetti - 2018 - Human Mutation - Wiley Online Library
Molecular basis and genetic testing strategies for diagnosing 21-hydroxylase deficiency, including CAH-X syndrome
