File:DNA Icon.svg
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| Date/Time | Thumbnail | Dimensions | User | Comment | |
|---|---|---|---|---|---|
| current | 10:46, 15 March 2018 |  | 70 × 78 (6 KB) | Palosirkka | fix |
| 20:30, 19 December 2007 |  | 70 × 78 (9 KB) | Fvasconcellos | {{Information |Description=Diagrammatic representation of a segment of a {{w|DNA}} strand. Meant for use as an icon. |Source=Adapted from Image:DNA replication editable.svg (a modification of Image:DNA replication.svg), by [[User:LadyofHats|Mari |
File usage
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.
- Scientific method
- Talk:Aase syndrome
- Talk:Abetalipoproteinemia
- Talk:Adducted thumb syndrome
- Talk:Adrenoleukodystrophy
- Talk:Albinism in humans
- Talk:Alpha-1 antitrypsin deficiency
- Talk:Androgen insensitivity syndrome
- Talk:Aneuploidy
- Talk:Angelman syndrome
- Talk:Asperger syndrome
- Talk:Ataxia–telangiectasia
- Talk:Autism spectrum
- Talk:Bardet–Biedl syndrome
- Talk:Biological inheritance
- Talk:Brugada syndrome
- Talk:Classical genetics
- Talk:Color blindness
- Talk:Congenital adrenal hyperplasia
- Talk:Crohn's disease
- Talk:Cystic fibrosis
- Talk:Cytogenetics
- Talk:Duane syndrome
- Talk:Epidermolysis bullosa
- Talk:Epigenetics
- Talk:Fabry disease
- Talk:Familial Alzheimer disease
- Talk:Familial adenomatous polyposis
- Talk:Fragile X syndrome
- Talk:Fructose malabsorption
- Talk:Gaucher's disease
- Talk:Genetic disorder
- Talk:Genetic marker
- Talk:Genetic testing
- Talk:Genomic imprinting
- Talk:Genomics
- Talk:Gilbert's syndrome
- Talk:Gulf War syndrome
- Talk:Haemophilia
- Talk:Har Gobind Khorana
- Talk:Harlequin-type ichthyosis
- Talk:Hereditary fructose intolerance
- Talk:Hereditary spastic paraplegia
- Talk:Hirschsprung's disease
- Talk:Homocystinuria
- Talk:Human behaviour genetics
- Talk:Hurler syndrome
- Talk:Inbreeding
- Talk:Inclusion body myositis
- Talk:Inflammatory bowel disease
- Talk:Kabuki syndrome
- Talk:Lactose intolerance
- Talk:Langer–Giedion syndrome
- Talk:Leber's hereditary optic neuropathy
- Talk:Lesch–Nyhan syndrome
- Talk:List of genetic disorders
- Talk:MOMO syndrome
- Talk:Malignant hyperthermia
- Talk:Marfan syndrome
- Talk:Medium-chain acyl-coenzyme A dehydrogenase deficiency
- Talk:Migraine
- Talk:Molecular biology
- Talk:Mucopolysaccharidosis
- Talk:Muscular dystrophy
- Talk:Neurofibromatosis type II
- Talk:Noonan syndrome
- Talk:Oncogene
- Talk:Ornithine transcarbamylase deficiency
- Talk:Osteogenesis imperfecta
- Talk:Pectus excavatum
- Talk:Peutz–Jeghers syndrome
- Talk:Pharmacogenetics
- Talk:Phenylketonuria
- Talk:Philadelphia chromosome
- Talk:Photic sneeze reflex
- Talk:Ploidy
- Talk:Polydactyly
- Talk:Porphyria
- Talk:Prader–Willi syndrome
- Talk:Prenatal testing
- Talk:Primary ciliary dyskinesia
- Talk:Progeria
- Talk:Quantitative trait locus
- Talk:Retinitis pigmentosa
- Talk:Rheumatoid arthritis
- Talk:Sex linkage
- Talk:Situs inversus
- Talk:Spina bifida
- Talk:Spinocerebellar ataxia
- Talk:Thalassemia
- Talk:Thanatophoric dysplasia
- Talk:Tourette syndrome
- Talk:Turner syndrome
- Talk:Williams syndrome
- Talk:Wolf–Hirschhorn syndrome
- Talk:XYY syndrome
- Talk:XY sex-determination system
- Talk:X chromosome
- Talk:Y chromosome
- User:Ianblair23/Sandbox
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- Benutzer:WissensDürster/Infothek
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- Portal:Biochemie/Exzellente Artikel
- Portal:Biochemie/Desoxyribonukleinsäure
- Benutzer Diskussion:DerGoSpieler
- Benutzer Diskussion:Samuel Pl
- Benutzer Diskussion:Stylidium
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- Benutzerin Diskussion:Anni S. Heins
- Portal:Pharmazie/Desoxyribonukleinsäure
- Portal:Pharmazie/Exzellente Artikel
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