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Abbreviation: CNVs
Appearance Frequency: 2930 time(s)
Long forms: 15

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Long Form No. Long Form Research Area Co-occurring Abbreviation PubMed/MEDLINE Info. (Year, Title)
copy number variations
(2829 times)
Genetics, Medical
(650 times)
SNPs (201 times)
CMA (152 times)
aCGH (138 times)
2006 Bias of selection on human copy-number variants.
Copy Number Variants
(60 times)
Genetics, Medical
(14 times)
ASD (4 times)
SNP (4 times)
ASDs (3 times)
2007 Systematic prediction and validation of breakpoints associated with copy-number variants in the human genome.
choroidal neovascularizations
(15 times)
Ophthalmology
(12 times)
OCT (7 times)
AMD (5 times)
RPE (4 times)
2001 Optical coherence tomography (OCT) findings in normal retina and laser-induced choroidal neovascularization in rats.
choroidal neovascular membranes
(7 times)
Ophthalmology
(7 times)
AMD (2 times)
ICG (1 time)
OCT (1 time)
1995 Indocyanine green angiography and choroidal neovascularization obscured by hemorrhage.
contingent negative variations
(7 times)
Neurology
(6 times)
AEP (1 time)
BPs (1 time)
ECDs (1 time)
1975 Reliability of the contingent negative variation and the auditory evoked potential.
choroidal new vessels
(3 times)
Ophthalmology
(3 times)
AMD (2 times)
RPE (2 times)
BCVA (1 time)
1999 Drusen in age-related macular degeneration: pathogenesis, natural course, and laser photocoagulation-induced regression.
canine noroviruses
(1 time)
Allergy and Immunology
(1 time)
--- 2014 Seroprevalence of canine norovirus in 14 European countries.
cell-engineered nanovesicles
(1 time)
Biocompatible Materials
(1 time)
ESC (1 time)
2017 Cell-Engineered Nanovesicle as a Surrogate Inducer of Contact-Dependent Stimuli.
chromosome number variations
(1 time)
Medicine
(1 time)
SILAC (1 time)
SNP (1 time)
2013 Proteomic and genomic analyses of antimony resistant Leishmania infantum mutant.
10  Classic neovessels
(1 time)
Ophthalmology
(1 time)
--- 2003 [Alternative therapies for choroidal neovessels resulting from age-related macular degeneration].
11  copy number genetic variants
(1 time)
Molecular Biology
(1 time)
PEIC (1 time)
2020 Genetic copy number variants, cognition and psychosis: a meta-analysis and a family study.
12  copy number structural variations
(1 time)
Neoplasms
(1 time)
BL (1 time)
EBV (1 time)
NGS (1 time)
2016 Genome-wide Analysis of Epstein-Barr Virus (EBV) Integration and Strain in C666-1 and Raji Cells.
13  copy number variations detected
(1 time)
Pediatrics
(1 time)
--- 2015 Microarray-based comparative genomic hybridization analysis in neonates with congenital anomalies: detection of chromosomal imbalances.
14  duplications-copy number variations
(1 time)
Reproductive Medicine
(1 time)
PGD-A (1 time)
2017 Diagnosis and clinical management of duplications and deletions.
15  PurposeCopy-number variants
(1 time)
Genetics, Medical
(1 time)
CRISPR (1 time)
2018 Noncoding copy-number variations are associated with congenital limb malformation.