Biochemistry, Genetics and Molecular Biology
Exome Sequencing
100%
Proband
51%
Promoter Region
51%
Embryonic Stem Cell
36%
Candidate Gene
36%
Genetic Heterogeneity
34%
Exome
33%
Sanger Sequencing
32%
FLT4
31%
Autosomal Recessive Disorder
31%
Protein Interaction
31%
Cardiac Muscle Cell
28%
Prevalence
28%
Transfer RNA
25%
Next Generation Sequencing
19%
GATA6
19%
Dysplasia
19%
Kinase Insert Domain Receptor
19%
Transcription Factors
17%
Genetic Divergence
16%
Protein Structure
15%
Interactome
15%
Pleiotropy
14%
Amelogenesis
14%
Downregulation
14%
Loss of Function Mutation
14%
Genome Wide Association Study
14%
Vascularization
12%
Ceramide
12%
Whole Genome Sequencing
12%
Compound Heterozygosity
12%
Biogenesis
12%
Missense Mutation
12%
Genetic Risk
12%
Germline
12%
Peptide Sequence
12%
Electronic Health Record
12%
Gene Locus
12%
Mitochondrial Protein
12%
Progeny
12%
ORAI1
12%
Hydrolase
12%
Germ Cell
12%
Induced Pluripotent Stem Cell
12%
Cognition
12%
Gene Analysis
12%
PEX1
12%
Peroxisome
12%
Karyotype 46,XX
12%
Genome-Wide Association Study
12%
Medicine and Dentistry
Diseases
35%
Persistent Truncus Arteriosus
25%
Clinical Feature
17%
Gain of Function Mutation
15%
Tetralogy of Fallot
12%
Lymph Duct
12%
Cellular Mechanism
12%
Exome Sequencing
12%
Transcription Factor GATA 6
12%
COVID-19
12%
UK Biobank
12%
Growth Retardation
12%
Hypertelorism
12%
Interferon
12%
Channel Gating
12%
Pernio
12%
Lupus Erythematosus
12%
Differential Diagnosis
12%
Autosomal Recessive Disorder
12%
Child
12%
Postnatal Growth
12%
Myopathy
12%
Anterior Chamber of Eyeball
12%
Pleiotropy
12%
Eyebrow
12%
Genitourinary System
12%
Cleft Lip Palate
12%
Absence
12%
Velopharyngeal Inadequacy
12%
Exome
12%
Lower Jaw
12%
Amelogenesis Imperfecta
12%
Interferon Type I
12%
Genetic Heterogeneity
12%
Epileptic Seizure
8%
Milroy's Disease
7%
In Vitro
7%
Receptor
7%
Skin Defect
6%
Congenital Malformation
6%
Hypoplasia
6%
Signaling Molecule
6%
Fetus Echography
6%
Glutamine
6%
Genetic Screening
6%
Edentulism
6%
Antivirus Agent
6%
Double Stranded RNA
6%
Prematurity
6%
Neurologic Disease
6%