Biochemistry, Genetics and Molecular Biology
Cytogenetics
100%
Karyotype
48%
Array Comparative Genomic Hybridization
44%
Chromosomal Abnormalities
43%
Mouse
34%
Haploinsufficiency
32%
Chromosome 6
29%
Fluorescence in Situ Hybridization
28%
Microarrays
28%
Chromosome 3
26%
Genetics
25%
Chromosome 1
25%
Body Height
22%
Copy-Number Variation
21%
Cancer Cell
21%
Candidate Gene
19%
Prevalence
19%
Trisomy
17%
Problem Behavior
16%
Intellectual Disability
15%
GRIN2A
14%
Ploidy
14%
Microdeletion Syndrome
13%
Genotype Phenotype Correlation
11%
Promoter Region
11%
Autosome
11%
Mosaicism
10%
Somatic Cell
10%
Southern Blotting
10%
Uniparental Disomy
10%
Loss of Heterozygosity
10%
Microsatellite DNA
9%
Y Chromosome
9%
Chromosome 15
8%
Flow Cytometry
8%
Chromosome Band
8%
Cognition
8%
Monosomy
8%
Genotyping
8%
Subtelomere
7%
Chromosomal Translocation
7%
Telomere
7%
Genetic Heterogeneity
7%
Chromosome 12
7%
EXT1
7%
Germline
7%
Germ Cell
7%
TBX1
7%
Chromosome Instability
7%
Chromosome Rearrangement
7%
Medicine and Dentistry
Neoplasm
43%
Chromosome Analysis
32%
Renal Oncocytoma
28%
Oncocytoma
23%
Chromosome 1
21%
Social Media
21%
Chromosome Aberration
18%
Diagnosis
18%
Karyotype
17%
Chromosome 6
16%
Tumor Cell
16%
Cancer
14%
Congenital Heart Defect
14%
Chromosome 3
11%
Developmental Delay
10%
Clear Cell
10%
Heterozygosity
10%
Clinician
9%
Cancer Cell
9%
Epileptic Seizure
8%
Congenital Malformation
8%
Congenital Disorder
7%
Y Chromosome
7%
Renal Cell Carcinoma
7%
Sarcomatoid
7%
Renal Adenoma
7%
Homeobox
7%
Autosomal Recessive Inheritance
7%
Identified Patient
7%
Horseshoe Kidney
7%
Uniparental Disomy
7%
Chromosome Change
7%
Plexiform Neurofibroma
7%
GRIN2A
7%
Myxosarcoma
7%
Chromophobe Adenoma
7%
Neurofibromatosis
7%
Adenoma
7%
Limb
7%
Psychomotor Retardation
7%
Coloboma
7%
Haploinsufficiency
7%
Metastatic Carcinoma
7%
Dysmorphic Feature
7%
Arm
7%
Immunohistochemistry
7%
Lymphoma Cell
7%
Cell Line
7%
Vimentin
7%
Carcinoid
7%
Keyphrases
Renal Oncocytoma
21%
Cardiac Myxoma
14%
Renal Cell Carcinoma
14%
Tumor
10%
Molecular Characterization
9%
Copy number Gain
8%
Chromosomal Patterns
8%
Cytological Changes
7%
Chromosomal Instability
7%
Exon Deletion
7%
Clinical Characterization
7%
17p13.3 Microduplication
7%
17p13.3 Microdeletion
7%
Genome-wide Array Analysis
7%
Aided Analysis
7%
Social Responsiveness Scale
7%
Laryngomalacia
7%
POMGNT1
7%
15q11.2
7%
Online Sources
7%
Neurexin
7%
Routine Diagnostics
7%
Breakage Characterisation
7%
Chromophobe
7%
XY Sex Reversal
7%
Nablus Mask-like Facial Syndrome
7%
Postaxial Polydactyly
7%
NR5A1 Gene
7%
46 XY Female
7%
Practical Guidelines
7%
Chromosome 7q
7%
CNTN4
7%
Molecular Cytogenetic Analysis
7%
Indicative Features
7%
High-resolution Arrays
7%
Autosome Translocation
7%
Human Larynx
7%
Mouse Lymphoma Cells
7%
Clinical Outcomes
7%
Previously Untreated
7%
Renal Cancer
7%
Mutation Analysis
7%
Soft Tissue Sarcoma
7%
Sarcomatoid
7%
Intracranial Teratoma
7%
Oncocytoma
7%
Chromosomal Region
7%
TP53 mutation
7%
Sequence Deletion
7%
Diffuse Neurofibroma
7%