Medicine and Dentistry
Bone Density
77%
Hypophosphatasia
75%
Bone Strength
64%
Bone Turnover
57%
Diseases
54%
Point Mutation
54%
Case-Control Study
50%
Bone Mass
49%
Cortical Bone
45%
Ossification
44%
Albers Schoenberg Disease
39%
Symptom
35%
Short Stature
33%
Disorders of Mitochondrial Functions
33%
Osteolysis
30%
Dual-Energy X-Ray Absorptiometry
30%
Distal Radius
30%
Diabetes Mellitus
29%
Nephropathy
27%
Cross Sectional Study
26%
Clinical Feature
25%
Multiple Endocrine Neoplasia
25%
Carisoprodol
25%
Trabecula
25%
Multiple Fracture
25%
Pycnodysostosis
25%
Fracture Healing
25%
Bone Malformation
25%
Hypogonadotropic Hypogonadism
25%
Clinical Genetics
25%
Counseling
25%
Proteinase
25%
Hypoparathyroidism
25%
Renal Failure
25%
Microcephaly
25%
Multiple Endocrine Neoplasia Type I
25%
Brain Tumor
25%
Cone Dystrophy
25%
Buccal Mucosa
25%
Hybrid Gene
25%
Eye Disease
25%
Drug Resistant Epilepsy
25%
Parathyroid Hormone
25%
Epileptic Absence
25%
Stem Cell
25%
Gene Mutation
25%
Diet Therapy
25%
Vagus Nerve Stimulation
25%
Drug Therapy
25%
DNA Mutation
25%
Biochemistry, Genetics and Molecular Biology
Mutational Load
100%
Point Mutation
78%
DNA Mutation
75%
Mitochondrial DNA
75%
Bone Density
50%
Prevalence
43%
Genetics
41%
Bone Mass
41%
Genetic Screening
40%
Germline
37%
ALPL
37%
Germ Cell
37%
Insulin Resistance
37%
Bone Strength
37%
Case-Control Study
33%
CDKN1B
33%
Insulin Release
33%
Glucose Tolerance Test
33%
Glucose Test
33%
Buccal Mucosa
31%
Missense
28%
RELA
25%
OPN1LW
25%
Leigh's Disease
25%
Retinitis pigmentosa
25%
ATP Synthase
25%
Insulin Sensitivity
25%
IKBKG
25%
X-Linked Hypophosphatemia
25%
Rickets
25%
Phosphorylase
25%
Glucose Homeostasis
25%
Bone Turnover
25%
Transfection
25%
Glucose Metabolism
25%
Genetic Trait
25%
Gene Mutation
25%
Porosity
22%
Alkaline Phosphatase
21%
Mitochondrial Myopathy
18%
Insulin Response
16%
X Ray
14%
Osteoclast
14%
Transfer RNA
12%
Proband
12%
Genetic Disorder
12%
Genetic Carrier
12%
Autosomal Recessive Inheritance
12%
Body Height
12%
Mitochondrial Genome
12%
Keyphrases
Permanent Hypoparathyroidism
25%
PNPLA6
25%
Adult Siblings
25%
Mitochondrial tRNA mutations
25%
Mutation Load
25%
Mitochondrial Myopathy
25%
Genetic Network
25%
Multiple Endocrine Neoplasia Type 4
25%
SHOX Gene
25%
IKBKG
25%
Tissue-specific Distribution
25%
RNU4ATAC
25%
Hypophosphatasia
25%
Microcephalic Osteodysplastic Primordial Dwarfism
25%
Minor Spliceosome
25%
Rearranged during Transfection
25%
PHKA2
25%
Impact Microindentation
25%
Ketotic Hypoglycemia
25%
LEMD3
25%
Pycnodysostosis
25%
Oligosymptomatic
25%
Phosphorylase
25%
Impaired Glucose Homeostasis
25%
Ataxia
25%
Retinitis pigmentosa
25%
Muscle Phenotype
25%
NARP Syndrome
25%
Buschke-Ollendorff Syndrome
25%
Modeling-based Bone Formation
25%
Formation Transformation
25%
Mitochondrial mutations
25%
Denmark
25%
Clinical Genetics
25%
Adults with Epilepsy
25%
Diet Therapy
25%
Telomere Dysfunction
25%
Epilepsy Surgery
25%
Jean Genet
25%
Blue Cone Monochromacy
25%
X Chromosome Inactivation
25%
Case-comparison Study
25%
Expert Collaboration
25%
Genetic Condition
17%
Abnormal muscle Response
16%
Clinical Follow-up
12%
Whole Genome Sequencing
12%
National Network
12%
Good Clinical Practice
12%
Healthcare Providers
12%
