Medicine and Dentistry
Patient
61%
Adult
54%
Mitochondrial DNA
45%
Hypophosphatasia
35%
Bone
34%
Mutational Load
33%
Diagnosis
29%
Therapeutic Procedure
28%
DNA Mutation
28%
Bone Density
27%
Association
26%
Phenotype
26%
Age
24%
Prevalence
24%
Disorders of Mitochondrial Functions
22%
Muscle
21%
Point Mutation
21%
Diseases
20%
Bone Strength
20%
Diabetes
20%
Diabetes Mellitus
19%
Person
18%
Tissues
18%
Bone Mass
17%
Gene
17%
Cortical Bone
16%
Child
15%
Female
14%
Hearing Impairment
13%
Blood
13%
Ossification
13%
Inpatient
12%
Alkaline Phosphatase
12%
Clinical Feature
11%
Follow up
11%
Distal Radius
11%
Insulin Resistance
11%
Transfer RNA
11%
Ataxia
11%
Epilepsy
11%
Case-Control Study
11%
Maternally Inherited Diabetes and Deafness
11%
Myopathy
11%
Leukocyte
10%
Cross Sectional Study
10%
Bone Turnover
9%
Genetic Transfection
9%
Multiple Endocrine Neoplasia
9%
Parathyroid Hormone
9%
NARP Syndrome
9%
Biochemistry, Genetics and Molecular Biology
Mutation
100%
Phenotype
38%
Association
36%
Point Mutation
32%
Bone
26%
Age
24%
Transfection
18%
Mutational Load
18%
Mitochondrial DNA
18%
Prevalence
16%
Ossification
15%
Phosphate
15%
Bone Mass
15%
Alkaline Phosphatase
15%
Nested Gene
13%
Hearing
13%
Insulin Resistance
12%
Transfer RNA
12%
Genetic Screening
12%
Bone Density
12%
Buccal Mucosa
11%
Leukocytes
11%
Lysozyme
11%
Skewed X-Inactivation
10%
X-Inactivation
10%
Osteolysis
10%
Bone Turnover
9%
Parathyroid Hormone
9%
Codon
9%
OPN1LW
9%
X-Linked Recessive Inheritance
9%
IKBKG
9%
PHKA2
9%
Kinase
9%
DNA
9%
Hybrid Gene
9%
Bone Healing
9%
Case-Control Study
9%
Retinitis pigmentosa
9%
Endopeptidase
9%
Phosphorylase
9%
Electron Transport Chain
9%
Mitochondrial Disease
9%
Genetics
9%
Childhood
8%
Body Height
8%
Osteoclast
7%
Insulin Release
7%
Heteroplasmy
7%
Development
6%
