Medicina y ciencias biológicas
46,XY Disorders of Sex Development
7%
Acute Coronary Syndrome
7%
Age of Onset
6%
Alleles
13%
Alzheimer Disease
7%
Apraxias
13%
Ataxia
10%
Attention Deficit Disorder with Hyperactivity
29%
Cardiomegaly
10%
Ceroid Lipofuscinosis, Neuronal, 6
9%
Child
7%
Chromosomes, Human, X
7%
Clopidogrel
10%
Colombia
38%
Colorectal Neoplasms
7%
Computational Biology
18%
Congenital Pain Insensitivity
8%
Costs and Cost Analysis
8%
cyanocobalamin, pyridoxine, thiamine drug combination
10%
Cytochrome P-450 CYP2C9
10%
Delivery of Health Care
7%
Drug-Related Side Effects and Adverse Reactions
21%
Duchenne Muscular Dystrophy
12%
Dystrophin
11%
Ebstein Anomaly
14%
Electrocardiography
11%
Exome
42%
Exons
15%
Eye
9%
Fabry Disease
14%
Familial premature ovarian failure
10%
Forkhead Transcription Factors
10%
Fucosidosis
8%
Gene Frequency
12%
Genes
71%
Genetic Association Studies
14%
Genetic Counseling
7%
Genetic Profile
7%
Genome
9%
Genome-Wide Association Study
23%
Genomics
17%
Glycogen Storage Disease Type II
7%
Habitual Abortion
18%
Hemophilia A
7%
High-Throughput Nucleotide Sequencing
37%
Ichthyosis
9%
Infertility
8%
Kounis Syndrome
8%
LEOPARD Syndrome
8%
Long QT Syndrome
8%
Lupus Coagulation Inhibitor
9%
Mammalian Chromosomes
7%
Medical Students
9%
Meta-Analysis
15%
Missense Mutation
20%
Molecular Biology
7%
Mutation
82%
MutS Proteins
7%
Nervous System
6%
Neuronal Ceroid-Lipofuscinoses
7%
Non-Receptor Type 11 Protein Tyrosine Phosphatase
8%
origen
8%
Pain
9%
Pandemics
8%
Pathology
8%
Peripheral Nervous System Diseases
9%
Pharmaceutical Preparations
14%
Pharmacogenetics
29%
Pharmacogenomic Testing
10%
Pharmacogenomic Variants
7%
Pharmacovigilance
7%
Phenotype
34%
placental alkaline phosphatase
7%
Point Mutation
9%
Polymerase Chain Reaction
6%
Population
22%
Pre-Eclampsia
14%
Pregnancy
15%
Primary Hypertrophic Osteoarthropathy
8%
Primary Ovarian Insufficiency
100%
Proteins
11%
Pyridoxine
15%
Quantitative Trait Loci
19%
RNA Splice Sites
8%
SARS Virus
9%
Self Medication
8%
Sequence Analysis
9%
Single Nucleotide Polymorphism
12%
Spontaneous Abortion
11%
Steroid 21-Hydroxylase
7%
Stevens-Johnson Syndrome
12%
Therapeutics
12%
Thiamine
18%
Transcription Factors
10%
Vitamin B 12
19%
Vitamin B 6
10%
Vitamin B Complex
26%
Warfarin
15%
Whole Exome Sequencing
37%
X Chromosome
13%