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File:Plain DNA icon.svg
From WikiMD's Food, Medicine & Wellness Encyclopedia
Size of this PNG preview of this SVG file: 64 × 64 pixels. Other resolution: 2,048 × 2,048 pixels.
Original file (SVG file, nominally 64 × 64 pixels, file size: 295 bytes)
File history
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Date/Time | Thumbnail | Dimensions | User | Comment | |
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current | 11:30, 8 March 2018 | 64 × 64 (295 bytes) | Sarang | {{Information |description={{en|1=Simple DNA icon; shows one segment of a {{w|DNA}} strand.}} |date=2018-03-08 |source={{own}} |author={{ut|Sarang}} |Other fields={{Igen|4=i|9=+|10=S}} }} =={{int:license-header}}== {{PD-ineligible}} Category:DNA helix-structures Category:Biology icons Category:Plain black SVG icons |
File usage
The following file is a duplicate of this file (more details):
- File:Plain DNA icon.svg from Wikimedia Commons
More than 100 pages use this file. The following list shows the first 100 pages that use this file only. A full list is available.
- 3' end
- 5' untranslated regions
- Additive genetic effects
- Admixture mapping
- Agar gel electrophoresis
- Allele
- Allelic heterogeneity
- Alpha thalassemia trait
- Alternative splicing
- Ames test
- Amino acid substitution
- Antihemophilic factor
- Antisense strand
- Autosomal chromosome
- Autosomal dominant
- Autosome
- B chromosomes
- Base sequence
- Base sequence analysis
- Branch migration
- Bronze diabetes
- CRISPR
- Cafe au lait spot
- Centromere
- Christmas disease
- Chromosomal abnormality
- Chromosomal deletion
- Chromosomal inversion
- Chromosome 17
- Chromosome 3
- Chromosome 7
- Chromosome analysis
- Chromosome banding
- Chromosome painting
- Chromosome pairing
- Chromosome puff
- Chromosome segregation
- Chromosome translocation
- Comparative genomic hybridization
- Congenital dyserythropoietic anemia
- Congenital hypogonadotropic hypogonadism
- Copy number variation
- DNA damage
- DNA fingerprinting
- DNA repair genes
- Double-pair mating
- Excision repair
- Flow karyotyping
- Full gene sequence
- Gene banks
- Gene expression regulation
- Gene flow
- Gene frequency
- Gene interaction
- Gene knockin
- Gene mapping
- Gene splicing
- Gene targeting
- Generalized lipodystrophy
- Genetic marker
- Genetic mosaic
- Genome sequence
- Genotyping
- HCT116 cells
- Hemoglobin c disease
- Hereditary disease
- Heritable disease
- Heterolactic fermentation
- Homeobox genes
- Initiation codon
- Insertional mutation
- Knockin
- Leader sequence
- Leaky mutant
- Linked genes
- Longer
- Mendelian inheritance
- Metatranscriptomics
- Methylation specific oligonucleotide microarray
- Missense mutation
- Mutagens
- Mutate
- Mutation
- Nucleotide salvage
- Prenatal diagnosis
- Regulon
- Repeat
- Steatocystoma
- Subclade
- Substitution mutation
- Tandem duplication
- Tandem repeat sequences
- Temperate phage
- Transposition
- Tumor-suppressor gene
- Unaffected
- Vasopressin-resistant diabetes insipidus
- Vertical gene transfer
- X-linked
- X-linked dominant
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