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Keyword [21 hydroxylase deficiency]
Result: 21 - 35 | Page: 2 of 2
21.
Genetic Analysis And Prenatal Diagnosis Of Congenital Adrenal Hyperplasia Due To 21-hydroxylase Deficiency
22.
Clinical Presentation And Mutational Spectrum In A Series Of 166 Patients With Classical 21-hydroxylase Deficiency From South China
23.
The Study Of The Correlation Between Postmenopausal Osteoporosis And Plasma Aldosterone/renin/the Study Of The Correlation Between Indole And Type 2 Diabetes/a Case Report Of 21-hydroxylase Deficiency
24.
The Relationship Between The Genotype And Clinical Phenotype With 21-hydroxylase Deficiency (21-OHD), And The Discussion Of The Three Unreported Mutations
25.
Clinical Characteristics Analysis Of 65 Patients With 21-hydroxylase Deficiency In Different ACTH Levels
26.
Molecular Genetic Study Of The Family Of Patients With Congenital Adrenal Hyperplasia
27.
Clinical Analysis Of 4 Cases Of Testicular Adrenal Rest Tumor
28.
Clinical Analysis And Genotype-phenotype Study Of 21-hydroxylase Deficiency
29.
Clinical Data And Genetic Analysis Of 56 Cases Of Congenital Adrenal Hyperplasia
30.
Multi-site Rapid Detection Of Deletion Genetic Diseases
31.
Progress Of Treatment For 21-hydroxylase Deficiency
32.
Identification Of Nonclassical 21-hydroxylase Deficiency And Polycystic Ovary Syndrome
33.
Noninvasive Prenatal Diagnosis Of Disorders Of Sex Development By Maternal Plasma DNA Sequencing
34.
Correlation Between Genotype And Phenotype Of 21-hydroxylase Deficiency
35.
Prenatal Dexamethasone Treatment For Congenital Adrenal Hyperplasia
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