Keyphrases
Russian Population
100%
Exome
100%
Wound Cleaning
100%
Scarce Resources
100%
St. John's Wort
100%
Protein-truncating Variants
100%
Acute Respiratory Distress Syndrome
100%
Recurrent Disease
100%
North America
100%
Randomized Trial
100%
Randomized Controlled Trial
100%
Cause of Disease
100%
White Oak
83%
Medical Genetics
50%
Adrenogenital Syndrome
50%
CYP21A2
50%
LCHAD Deficiency
50%
Missense mutation
50%
Genetic Behavior
50%
Xeroderma pigmentosum
50%
Alpha-1 Antitrypsin Deficiency
50%
Disease Genes
50%
Benefit Claiming
50%
Classical Form
50%
ATP7B
50%
Acral Peeling Skin Syndrome
50%
PROP1
50%
Supercritical CO2 (SCO2)
50%
VLCAD Deficiency
50%
ACADVL
50%
Sensorineural Deafness
50%
Complement Component 2
50%
CatSper1
50%
Population Control
50%
Pituitary Hormone Deficiency
50%
Cytochrome c Oxidase Deficiency
50%
ClinVar
50%
Von Willebrand Disease
50%
Recessive Disease
50%
SERPINA1
50%
Spermatogenic Failure
50%
HADHA
50%
Retinitis pigmentosa
50%
Complement Components
50%
Amino Acid Substitution
50%
Genetic Studies
50%
Staphylococcus Aureus
50%
Disease Pattern
50%
Wilson Disease
50%
Tap Water
33%
Biochemistry, Genetics and Molecular Biology
Exome
100%
Randomized Controlled Trial
100%
Allele
100%
Medline
50%
PROP1
33%
SCO2
33%
Retinitis pigmentosa
33%
Cytochrome C Oxidase
33%
Complement Component 2
33%
HADHA
33%
Pituitary Hormone
33%
Medical Genetics
33%
Von Willebrand Factor
33%
ACADVL
33%
Von Willebrand Disease
33%
Xeroderma pigmentosum
33%
Alpha 1-Antitrypsin
33%
Missense Mutation
33%
Population Dynamics
33%
Genetics
33%
Amino Acid Substitution
33%
Data Extraction
25%
Prevalence
25%
Medicine and Dentistry
Exome
100%
Allele
100%
Recurrent Disease
100%
Congenital Adrenal Hyperplasia
33%
Index Case
33%
Alpha 1-Antitrypsin Deficiency
33%
Chemexfoliation
33%
Cytochrome C Oxidase Deficiency
33%
Von Willebrand Disease
33%
Complement Component C2
33%
Hypophysis Hormone
33%
Population Dynamics
33%
Hormone Deficiency
33%
Xeroderma pigmentosum
33%
Missense Mutation
33%
Retinitis pigmentosa
33%
Complement
33%
Amino Acid Substitution
33%
Von Willebrand Factor
33%
Sensorineural Hearing Loss
33%
Wilson's Disease
33%
Disease
33%
