INIS
patients
100%
lungs
67%
diseases
50%
genes
48%
sex
39%
cancer
33%
colombia
33%
adenocarcinomas
22%
tissues
21%
karyotype
18%
transcription factors
17%
females
16%
fishes
16%
genetics
14%
tumors
14%
hospitals
13%
in-situ hybridization
13%
fluorescence
13%
management
13%
oxygen
13%
correlations
12%
enrichment
12%
males
12%
rna
11%
ducts
11%
symptoms
11%
blood
11%
covid-19
11%
defects
11%
sarcomas
11%
barriers
11%
lymphomas
11%
kinases
11%
biological markers
11%
surges
11%
osteoblasts
11%
mortality
11%
oncogenes
11%
interstitials
11%
saturation
10%
distance
9%
levels
8%
anemias
8%
phenotype
8%
etiology
7%
mosaicism
6%
congenital diseases
6%
promoters
6%
variations
6%
kidneys
5%
surgery
5%
metaphase
5%
gonads
5%
pathology
5%
Biochemistry, Genetics and Molecular Biology
Transcription Factors
30%
Genetics
28%
Bioinformatics
26%
SOX9
26%
Epigenetics
24%
Gene Expression Profiling
23%
Cytogenetics
23%
Karyotype
22%
Epigenetic Mechanism
18%
Gonad Development
18%
Multiplex Ligation-Dependent Probe Amplification
18%
Promoter Region
17%
Fluorescence in Situ Hybridization
17%
Transcription Factor RUNX
16%
Copy-Number Variation
14%
SRY Gene
14%
Gene Expression
13%
Chromosomal Abnormalities
13%
Gene Dosage
13%
Transcription
13%
Tumor Gene
12%
Gene Mutation
12%
Sex Differentiation
11%
Long Noncoding RNA
11%
Periostin
11%
Anaplastic Lymphoma Kinase
11%
Karyotype 47,XXY
11%
RUNX2
11%
Mosaicism
11%
Oncogene
11%
Tumor Suppressor Protein
11%
Gene Regulatory Network
11%
Ewing Sarcoma
11%
Osteoblast
11%
Transgenic Mouse
11%
C9orf72
11%
Astrocyte
11%
Real-Time Polymerase Chain Reaction
9%
Genetic Determinism
8%
Embryogenesis
7%
SOX3
7%
Karyotyping
7%
Transcriptomics
6%
Klinefelter Syndrome
6%
Karyotype 46,XY
6%
Sex Chromosome
5%
Teratoma
5%
Downregulation
5%
Testis Development
5%
Tracheoesophageal Fistula
5%
Hub Genes
5%
Shear Stress
5%
Cell Function
5%
Candidate Gene
5%
WT1
5%
Array Comparative Genomic Hybridization
5%
Decision Support System
5%
Comorbidity
5%
Transcriptome
5%
Mouse Model
5%
Keyphrases
Müllerian Structures
11%
Compound Heterozygous mutation
11%
Persistent Müllerian Duct Syndrome
11%
Runt-related Transcription Factor 2 (Runx2)
11%
Master Genes
11%
H3K4me3
11%
COMPASS Complex
11%
Osteoblast
11%
Barriers to Access
11%
Oncogene
11%
Anaplastic Lymphoma Kinase
11%
Anaplastic Lymphoma Kinase Gene
11%
Lung Adenocarcinoma
11%
Ewing Sarcoma
11%
Characteristic number
11%
VACTERL Association
11%
Fanconi Anemia
11%
RUNX Family
11%
Oncogenic Process
11%
Tumor Suppressor
11%
Genetic Characterization
11%
Patient Cohort
11%
Cytogenetic Characterization
11%
Persistent Symptoms
11%
Severe COVID-19 Infection
11%
Lung-other
11%
BAC Transgenic Mice
11%
H3K9me3
11%
Transcriptional Targets
11%
SRY Gene
11%
Chromosomal Genes
11%
Gene Finding
11%
Lung Cancer Biomarkers
11%
47,XXY
11%
Gonadal Dysgenesis
11%
Klinefelter
11%
XYY Syndrome
11%
Barriers in Access
7%
Distance Walked
7%
Klinefelter Syndrome
6%
Uterus
5%
Anti-Müllerian Hormone
5%
Bilateral Cryptorchidism
5%
Adult Male
5%
Phenotypic Male
5%
Incidental
5%
Fallopian Tube
5%
AMHR2 Gene
5%
Abdominal Mass
5%
Cryptorchidism
5%
Regulatory Ability
5%
Oncogenic Potential
5%
Chromosome 2
5%
Pathology Department
5%
ALK Inhibitor
5%
Lung Cancer Patients
5%
2 Regions
5%
Anaplastic Lymphoma Kinase Rearrangement
5%
Short-arm
5%
IHC Assay
5%
NSCLS
5%
Paraffin-embedded Samples
5%
FISH Assay
5%
Limb Defects
5%
Choanal Atresia
5%
Master Regulator
5%
Dual Function
5%
Diagnostic Interventions
5%
Oncogenic Signaling
5%
Whole Family
5%
Developmental Programming
5%
Biological Characteristics
5%
Runt-related Transcription Factor
5%
Molecular Study
5%
Transcription Factor Family
5%
Vertebral Abnormalities
5%
Gonadal Differentiation
5%