21 hydroxylase deficiency - Globe Thesis

Keyword [21 hydroxylase deficiency] Result: 1 - 20 \| Page: 1 of 2
1.	Study On The Clinical Characteristics And The Genetic Mutations Of 17α-hydroxylase/17, 20-lyase Deficiency
2.	.21 Hydroxylase Deficiency - Rapid Genetic Diagnosis, As Well As Genotypic And Phenotypic Study Of The Relationship
3.	.21 - Hydroxylase Deficiency, Clinical And Genetic Diagnosis
4.	Disorders Of Sex Differentiation In Female Caused By Congenital Adrenal Hyperplasia: Analysis Of 8 Cases
5.	Molecular Genetic Analysis Of Chinese Families With 21-Hydroxylase Deficiency
6.	CYP21A2 Gene Diagnosis Of Congenital Adrenal Hyperplasia
7.	Rapid Molecular Diagnosis Of Congenital Adrenal Hyperplasia Due To 21-hydroxylase Deficiency
8.	High Progesterone Hyperlipidemia Clinical And Basic Research
9.	A Novel Point Mutation In The CYP21A2Gene Identified In A Chinese Han Patient With Nonclassic21-hydroxylase Deficiency
10.	17α-hydroxylase And21-hydroxylase:the Case Report And Literature Review
11.	Establishment And Application Of A Method For Gene Diagnosis Of 21-hydroxylase Deficiency
12.	Analysis Of Etiology And Clinical Characteristics In Patients With Gonadal Function Disorders
13.	Study Of Genotype And Phenotype Among Uyghur Children With 21- Hydroxylase Deficiency In Xinjiang
14.	The Functional Characterization Study Of CYP21A2 Gene Mutation Causing 21-hydroxylase Deficiency In One Pedigree
15.	Genotype And Clinical Phenotype In Classical 21-Hydroxylase Deficiency Patients
16.	Bilateral Testicular And Adrenal Tumors Leading To The Diagnosis Of Congenital Adrenal Hyperplasia:a Case Report And Literature Review
17.	The New Mutation Of CYP21A2 Gene And Congenital Adrenal Hyperplasia:A Case Report
18.	Correlation Analysis Of Genotype And Clinical Phenotype Of 21-hydroxylase Deficiency In Shanxi Province
19.	The Prognostic Effect Of Different Initial Treatment Age On The Patients With 21-hydroxylase Deficiency
20.	Functional And Structural Analysis Of Four Novel Mutations Of CYP21A2 Gene And Genotype-phenotype Correlation In 72 Chinese Patients With 21-hydroxylase Deficiency
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