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Keyword [CYP21A2]
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1. CYP21A2 Gene Diagnosis Of Congenital Adrenal Hyperplasia
2. Rapid Molecular Diagnosis Of Congenital Adrenal Hyperplasia Due To 21-hydroxylase Deficiency
3. The Relationship Between CYP21A2Polymorphism And Acne In The Han Ethnic Group
4. Association Study Of Genetic Variants In Androgen-Regulated Genes And Risk Of Severe Acne In Han Population From Southwest China
5. Establishment And Application Of A Method For Gene Diagnosis Of 21-hydroxylase Deficiency
6. The Functional Characterization Study Of CYP21A2 Gene Mutation Causing 21-hydroxylase Deficiency In One Pedigree
7. Genotype And Clinical Phenotype In Classical 21-Hydroxylase Deficiency Patients
8. Bilateral Testicular And Adrenal Tumors Leading To The Diagnosis Of Congenital Adrenal Hyperplasia:a Case Report And Literature Review
9. The New Mutation Of CYP21A2 Gene And Congenital Adrenal Hyperplasia:A Case Report
10. Analysis Of CYP21A2 Mutations In Children With Hyperandrogenemia
11. Correlation Analysis Of Genotype And Clinical Phenotype Of 21-hydroxylase Deficiency In Shanxi Province
12. Functional And Structural Analysis Of Four Novel Mutations Of CYP21A2 Gene And Genotype-phenotype Correlation In 72 Chinese Patients With 21-hydroxylase Deficiency
13. Genetic Analysis And Prenatal Diagnosis Of Congenital Adrenal Hyperplasia Due To 21-hydroxylase Deficiency
14. Clinical Presentation And Mutational Spectrum In A Series Of 166 Patients With Classical 21-hydroxylase Deficiency From South China
15. Establishment Of Gene Diagnostic Methods For Three Common Disorders Of Sex Development Disease
16. Clinical Analysis And Genotype-phenotype Study Of 21-hydroxylase Deficiency
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