Biochemistry, Genetics and Molecular Biology
Mouse
87%
Williams Syndrome
82%
Transcription Factors
79%
PAX3
53%
Elastin
50%
Autosomal Dominant Inheritance
43%
Genotyping
43%
Human Genome
40%
Multigene Family
37%
Copy-Number Variation
35%
Gene Dosage
32%
Candidate Gene
30%
Autosomal Recessive Disorder
30%
21-Hydroxylase
26%
Pax Genes
26%
Fusion Gene
26%
Microphthalmia-Associated Transcription Factor
26%
Transposable Element
26%
Transposase
26%
Exon
24%
Point Mutation
23%
Allele
23%
Genotype Phenotype Correlation
23%
Microarrays
22%
Haploinsufficiency
22%
Embryogenesis
22%
C-Terminus
21%
Transcription
20%
Missense
17%
Genetic Mechanism
17%
Craniofacial Development
17%
Surface Property
17%
Gene Structure
17%
Loss of Function Mutation
17%
Gene Cluster
16%
Gene Mutation
16%
Somatic Cell
16%
Molecular Lesion
16%
Secretory Pathway
15%
Cladistics
15%
Gene Expression
15%
Gene Conversion
14%
Gene Mapping
13%
Single Gene Disorder
13%
Morphology
13%
Golgi Apparatus
13%
Complement Component 4
13%
Stargazer Mouse
13%
Exome
13%
Wnt Signaling Pathway
13%
Neuroscience
Williams Syndrome
100%
Transcription Factors
34%
Pax Genes
26%
Face
16%
Cognitive Disorders
14%
Cystic Fibrosis Transmembrane Conductance Regulator
13%
Scaffold Protein
13%
Guanylate Kinase
13%
Skeletal Muscle
13%
Exon
13%
Fusion Gene
13%
Cystic Fibrosis
13%
Neurofibromatosis Type 1
13%
Gene Conversion
13%
Long Terminal Repeat
13%
Growth Differentiation Factor 6
13%
Haplotype
13%
Albinism
13%
Microsatellite
13%
Gene Expression
13%
Microphthalmia-Associated Transcription Factor
13%
Transposon
10%
Transposase
10%
Motor Coordination
10%
Chromosome 7
9%
Haploinsufficiency
6%
Obsession
5%
Human Cognition
5%
Medicine and Dentistry
Williams Beuren Syndrome
48%
Diseases
15%
Developmental Disorder
15%
Elastin
13%
Smooth Muscle Cell
13%
Transcription Factors
13%
Rapamycin
13%
Artery Disease
13%
Klippel Feil Syndrome
13%
Waardenburg Syndrome
13%
Contig
13%
Dysmorphology
13%
Heterozygote
13%
Infantile Spasm
13%
Growth Differentiation Factor 6
13%
Genome Sequencing
13%
Cognitive Defect
13%
Skeletal Muscle
13%
Cell Proliferation
13%
Erythropoiesis
13%
Literacy
13%
Gene Expression
13%
Mechanistic Target of Rapamycin
11%
Hemifacial Microsomia
8%
Congenital Disorder
8%
Microphthalmia Associated Transcription Factor
7%
Recurrence Risk
6%
Counseling
6%
Second Pharyngeal Arch
6%
Clinical Feature
6%
Spine
6%
Gene Frequency
6%
Clinical Management
6%
Embryo Development
6%
Development of the Ears
6%
Lower Jaw
6%
Supravalvular Aortic Stenosis
6%
Helix
5%