Keyphrases
Family Study
100%
P21 Gene
100%
Congenital Adrenal Hyperplasia
100%
21-Hydroxylase Deficiency (21OHD)
42%
Healthy Controls
14%
Prevalence Rate
14%
Genomic DNA (gDNA)
14%
Polymerase Chain Reaction
14%
Pseudogene
14%
21-hydroxylase
14%
Short-arm
14%
Severe Disease
14%
Restriction Fragment Length Polymorphism
14%
Major Histocompatibility Complex
14%
Solid Phase
14%
Leucine
14%
Codon
14%
Chromosome 6
14%
Direct Sequencing
14%
Coding Genes
14%
First Exons
14%
Large Deletion
14%
Sequence-specific Oligonucleotide
14%
Frequent mutation
14%
Neuroscience
Haplotype
100%
Hyperplasia
100%
Human Leukocyte Antigen
100%
Steroid 21 Monooxygenase
57%
Polymerase Chain Reaction
28%
Genomic DNA
14%
Exon
14%
Intron
14%
Codon
14%
Pseudogene
14%
Restriction Fragment Length Polymorphism
14%
Leucine
14%
Major Histocompatibility Complex
14%
Human Leukocyte Antigen Disease
14%
Chromosome 6
14%
Biochemistry, Genetics and Molecular Biology
Haplotype
100%
Human Leukocyte Antigen
100%
21-Hydroxylase
57%
Allele
14%
Oligonucleotide
14%
Intron
14%
Pseudogene
14%
Exon
14%
Codon
14%
Restriction Fragment Length Polymorphism
14%
Prevalence
14%
Leucine
14%
Major Histocompatibility Complex
14%
Chromosome 6
14%
Solid
14%
C4A
14%