Biochemistry, Genetics and Molecular Biology
Case Report
100%
Mutation
81%
Phenotype
68%
Adulthood
50%
Hormone Resistance
50%
Optics
50%
Missense
50%
Parathyroid Hormone
50%
Spectrum
31%
Exome Sequencing
31%
Nested Gene
31%
Protein
25%
Electron
25%
Computer Model
25%
Degradation
25%
Fluorescence Microscopy
25%
Autosomal Dominant Inheritance
25%
GTPase
25%
Western Blot
25%
Association
25%
Aging
25%
Bone
12%
Tooth Eruption
12%
Hypocalcaemia
12%
Bioinformatics
6%
Protein Conformation
6%
Epigenetics
6%
Calcium Carbonate
6%
Ossification
6%
Vitamin D
6%
Gene Analysis
6%
Age
6%
Sample
6%
Locus (Genetics)
6%
Alfacalcidol
6%
Medicine and Dentistry
Agenesis
56%
Olfactory Bulb
50%
Campomelic Dysplasia
50%
Disease
50%
Hormone Resistance
50%
Parathyroid Hormone
50%
Initiation Factor 2
33%
Microcephaly
33%
Phenotype
18%
Hypogonadism
16%
Clustered Regularly Interspaced Short Palindromic Repeat
16%
Initiation Factor
16%
Translation (Protein Synthesis)
16%
Gene
12%
Child
12%
Hypocalcaemia
12%
Tooth Eruption
12%
Hyperphosphatemia
12%
Haploinsufficiency
10%
Prenatal Diagnosis
10%
Hormone Determination
6%
Follow up
6%
Bone Age
6%
Osteopenia
6%
Protein Conformation
6%
Molecular Pathology
6%
Congenital Malformation
6%
Ossification
6%
Vitamin D
6%
Blood Sampling
6%
Face
6%
Diagnosis
6%
Distal Phalanx
6%
Patient
6%
Epigenomics
6%
Clinodactyly
6%
Parent
6%
Alfacalcidol
6%
Deciduous Teeth
6%
Analysis
6%
Epileptic Seizure
6%
Metacarpal Bone
6%
Aragonite
6%
Gene Locus
6%
Brain Ventricle Peritoneum Shunt
6%