Keyphrases
21-Hydroxylase Deficiency (21OHD)
100%
B Locus
100%
Biochemical Criteria
25%
Chorionic Villus Sampling
25%
Clinical Criteria
25%
Clinical Diagnosis
25%
Digestion
25%
DNA Probe
100%
Genomic DNA (gDNA)
25%
Genotype
50%
HLA-B
100%
HLA-B Gene
25%
Locus-specific
100%
MspI
100%
Non-carriers
50%
Nuclear Family
25%
Polymorphism
100%
Restriction Fragment Length Polymorphism
25%
Steroid 21-hydroxylase
25%
TaqI
50%
TaqI Polymorphism
25%
Biochemistry, Genetics and Molecular Biology
21-Hydroxylase
100%
Chorion Villus
20%
DNA Probe
100%
Genomics
20%
Genotyping
20%
HLA-B
100%
Restriction Fragment Length Polymorphism
20%
TaqI
60%
Immunology and Microbiology
Chorion Villus
33%
DNA Probe
100%
Restriction Fragment Length Polymorphism
33%
TaqI
100%