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Keyword [CYP21A2]
Result: 1 - 16 | Page: 1 of 1
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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