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- CYP17A1
- 21-
Hydroxylase - Hydroxylase
Deficiency - CYP21A2
- Heterozygous Gene
Mutation - 21-Hydroxylase
Deficient - Cah
Syndrome - 17 Alpha Hydroxylase
Deficiency - Chimeric
Gene - 21-Hydroxylase
Enzyme - Allele-Specific
PCR - CYP3A4
- Compound Heterozygous
Mutation - Homozygous
Mutation - Adrenal Cortical
Hyperplasia - Congenital
Hyperplasia - CYP21A2
Hybrid Gene - CYP21A2
Sequencing - 21 B
Hydroxylase - Estrogen Synthesis
Pathway - CYP21A2
Cyp21a1p - Adrenal Development
Gene - 21 Alpha
Hydroxlase - Chromosome
7 - CYP17A1
Inhibitors - Steroidogenesis
Pathway - 21-Hydroxylase
Steroid - Null
Allele - Gene
Structure - 21-Hydroxylase Deficiency
Salt Wasting - Cah Genetic
Disorder - CYP1A2 Gene
Mutation - Steroid Hormone
Pathway Chart - Chimera
Syndrome - Gene
Conversion Mutation - 21-Hydroxylase
Deficiency Labs - CYP
Gene - CYP2A6
Polymorphism - 视黄醇代谢
CYP4A - Mouse Gene
CYP1A1 Cardiovascular Disease - Phenotype and Genotype
Worksheet - NGS Gene
Panel Exome Sequence Sanger Sequence - Bowlin Mutation
Gene - Phenylketonuria
Chromosome 12 - PCR
Heterozygote - Photo of an Infant with CYP21A2 Mutation
- Cah
Disease - Cyp26a1
- CYP2C19
mRNA - 21B Hydroxylase
Deficiency
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