Biochemistry, Genetics and Molecular Biology
Array Comparative Genomic Hybridization
100%
Microarrays
53%
Genetics
44%
Exome Sequencing
40%
Missense
35%
Genotyping
32%
Preimplantation
30%
Filamin
30%
Homozygote
30%
Allele
29%
Genetic Screening
28%
Proband
22%
Mouse
21%
Vitamin K
21%
Intellectual Disability
21%
Messenger RNA
20%
Heterozygote
19%
Genetic Carrier
19%
Gene Linkage
19%
Gene Mutation
17%
Haploinsufficiency
16%
Developmental Stage
15%
X-Inactivation
15%
Tuberous Sclerosis
15%
Pedigree
15%
Genetic Disorder
15%
Wolfram Syndrome
15%
Pharmacoepidemiology
15%
Nebulin
15%
Nuclear Receptor Co-Repressor 1
15%
Preimplantation Embryo
15%
Rett Syndrome
15%
Diamond-Blackfan Anemia
15%
Exon
15%
Cytochrome
15%
Protein Biosynthesis
15%
Animal Model
15%
CYP2C9
15%
Binding Domain
15%
Autoantibodies
15%
Cystic Fibrosis
15%
Actin
15%
Biogenesis
15%
Penetrance
15%
Low Copy Repeats
15%
Monospecific Antibody
15%
Blastocyst
15%
Enzyme
15%
Robertsonian Translocation
15%
Paternal Age
15%
Keyphrases
Chromosomal Microarray
73%
Prenatal Diagnosis
45%
Fetus
35%
Warfarin
31%
Nurture
30%
Arrhythmogenic Cardiomyopathy
30%
High Risk
30%
Autoantibodies
26%
Homozygote
26%
Exome Sequencing
26%
Copy number Variation
25%
Neurodevelopmental Disorders
24%
Missense Variants
24%
Intellectual Disability
24%
Ashkenazi Jews
24%
Dermatomyositis
22%
Filamin A
22%
CYP2C9
21%
Molecular Diagnostics
20%
Clinical Phenotype
20%
Carrier State
20%
Ribosomopathy
20%
Tertiary Care Hospital
19%
Proband
19%
Diagnosis Treatment
19%
Individual Sensitivity
17%
Whole Exome Sequencing
16%
Dilated Cardiomyopathy
16%
Truncating mutation
16%
Haploinsufficiency
16%
Medical Center
15%
Nuclear Receptor
15%
Predictive Value
15%
Serum Ferritin
15%
Retinoic Acid Signaling
15%
Vitamin K1
15%
Related Disorders
15%
Familial Mediterranean Fever Patient
15%
Leadless Pacemaker
15%
Sinus Pause
15%
Amyopathic Dermatomyositis
15%
Excessive Anticoagulation
15%
Paraneoplastic
15%
International Normalized Ratio
15%
Treatment Response
15%
Progressive Fibrosing Interstitial Lung Disease (PF-ILD)
15%
Ultrasound Findings
15%
Neuropsychiatric Systemic Lupus Erythematosus (NPSLE)
15%
Screening Diagnosis
15%
Dominant mutation
15%
Medicine and Dentistry
Disease
47%
Ribosome
45%
Autoantibodies
33%
Array Comparative Genomic Hybridization
32%
Prenatal Diagnosis
30%
Interstitial Lung Disease
30%
Dermatomyositis
22%
Myopathy
17%
Protein Synthesis
15%
Rare Disease
15%
Hamartoma
15%
Heterozygote
15%
Pacemaker Implantation
15%
Malignant Neoplasm
15%
Myositis
15%
Ventricular Septal Defect
15%
Exon
15%
Paraneoplastic Cerebellar Degeneration
15%
Nemaline Myopathy
15%
Retinitis pigmentosa
15%
Diamond-Blackfan Anemia
15%
Biogenesis
15%
Homozygote
15%
Pervasive Developmental Disorder
15%
Posterior Fossa
15%
Ferritin
15%
Corpus Callosum
15%
Wolfram Syndrome
15%
Nebulin
15%
Sudden Death
15%
Fetus Echography
15%
Cardiomyopathy
15%
Pediatrics Patient
15%
Treatment Response
15%
Gene Mutation
15%
Molecular Diagnosis
13%
Symptom
11%
Raynaud Phenomenon
11%
Translating (Language)
11%
Filamin
11%
Patient Referral
10%
Diabetes
10%
Optic Nerve Atrophy
10%
Neonatal Infant
7%
Enhanced Green Fluorescent Protein
7%
Heart Block
7%
Luciferase
7%
Cysteine
7%
Eukaryotic Cell
7%
Escherichia coli
7%
