Biochemistry, Genetics and Molecular Biology
Excavata
100%
22q13 Deletion Syndrome
100%
Body Height
64%
Genetic Disorder
60%
Growth Hormone
50%
Bovine Somatotropin
50%
Ring Chromosome
50%
Genetic Variation
50%
Kinase
50%
Phosphotransferase
50%
Chromosome 22
50%
DNA Methylation
50%
Natriuretic Peptide
50%
Peptide Receptor
50%
Genetics
41%
C-Type Natriuretic Peptide
40%
Genetic Counseling
22%
Guanylate Cyclase
20%
CpG Site
20%
Genetic Screening
18%
International Classification of Functioning, Disability and Health
12%
Chromosomal Disorder
11%
SHANK3
11%
Bone Growth
10%
FANCA
10%
Crosslinking of DNA
10%
Alpha 1-Antitrypsin
10%
Knowledge Base
10%
DNA Repair
10%
Bone Marrow Failure
10%
Adenosine Triphosphate
10%
Gene Conversion
10%
Fibroblast
10%
Gene Mutation
10%
Wild Type
10%
Protein Modeling
7%
Maturation
7%
Genotype Phenotype Correlation
7%
Genetic Gain
5%
Clinical Trial
5%
Prevalence
5%
Comorbidity
5%
Tumor Suppressor Gene
5%
Karyotyping
5%
SMARCB1
5%
Decision Making
5%
Chromosomal Translocation
5%
N-Terminus
5%
Homology Modeling
5%
Eicosanoid Receptor
5%
Medicine and Dentistry
22q13 Deletion Syndrome
100%
Funnel Chest
100%
Recurrence Risk
50%
Genetic Disorder
50%
Systematic Review
50%
Counseling
50%
Growth Hormone
50%
Genetic Variation
50%
Chromosome 22
50%
Neoplasm
22%
Genetic Counseling
22%
Bone Age
21%
Genetic Screening
18%
Diseases
18%
Patient Referral
16%
Dysmorphic Feature
14%
Osteoarthritis
14%
Short Stature
14%
Health Care Provider
12%
International Classification of Impairments, Disabilities and Handicaps
12%
Pediatrics
12%
Clinician
11%
Recurrent Disease
11%
Brachydactyly
7%
Absence
7%
Genotype Phenotype Correlation
7%
Maturation
7%
Midface Hypoplasia
7%
Diagnosis
5%
Family History
5%
Genetic Analysis
5%
Congenital Heart Defect
5%
Decision Making
5%
Schwannomatosis
5%
Chromosome Aberration
5%
Neurofibromatosis Type II
5%
Neurodevelopmental Disorder
5%
Clinical Feature
5%
Tumor Suppressor Gene
5%
Prenatal Diagnostics
5%
Clinical Trial
5%
Atypical Teratoid Rhabdoid Tumor
5%
Surgery
5%
Prevalence
5%
Differential Diagnosis
5%
Chromosome Disorder
5%
Noonan Syndrome
5%
Connective Tissue Disease
5%
Outpatient
5%
Pediatric Surgery
5%