Biochemistry, Genetics and Molecular Biology
Nested Gene
100%
Mutation
57%
Chromosome
26%
Phenotype
25%
Mouse
25%
Protein
23%
Elastin
21%
Transcription Factor
20%
Williams Syndrome
19%
DNA
13%
PAX3
12%
Spectrum
12%
Autosomal Dominant Inheritance
12%
Genotyping
11%
Sequencing
9%
Point Mutation
9%
Microphthalmia-Associated Transcription Factor
9%
Multigene Family
9%
Copy-Number Variation
8%
Gene Dosage
8%
Gene Mutation
8%
Candidate Gene
7%
Electric Potential
7%
Human
7%
Experiment
7%
21-Hydroxylase
7%
Fusion Gene
7%
Genotype Phenotype Correlation
6%
Allele
6%
Screening
6%
Genetics
6%
Autosomal Recessive Disorder
6%
Cognition
6%
Mental Retardation
6%
Association
6%
Haploinsufficiency
5%
Age
5%
Growth
5%
Transcription
5%
Pax Genes
5%
Medicine and Dentistry
Gene
34%
Williams Beuren Syndrome
19%
Patient
18%
Elastin
18%
Family
16%
Chromosome
15%
Supravalvular Aortic Stenosis
13%
Syndrome
13%
Transcription Factor
10%
Inpatient
8%
Protein
8%
Analysis
8%
Developmental Disorder
7%
Fusion Gene
7%
Etiology
6%
Face
6%
Diseases
5%
Autosomal Dominant Inheritance
5%
Brain
5%
Phenotype
5%
Point Mutation
5%
