Image:DNA.png
From Wikipedia, the free encyclopedia
DNA.png (215KB, MIME type: image/png
)
[edit] Summary
Modified from http://www.genome.gov/pressDisplay.cfm?photoID=96
[edit] Licensing
I, the creator of this work, hereby release it into the public domain. This applies worldwide.
In case this is not legally possible,
I grant any entity the right to use this work for any purpose, without any conditions, unless such conditions are required by law.
File history
Legend: (cur) = this is the current file, (del) = delete
this old version, (rev) = revert to this old version.
Click on date to download the file or see the image uploaded on that date.
- (del) (cur) 17:10, 10 July 2006 . . Apers0n (Talk | contribs) . . 586×443 (219,961 bytes) (Modified from http://www.genome.gov/pressDisplay.cfm?photoID=96)
- Edit this file using an external application
See the setup instructions for more information.
File links
The following pages on the English Wikipedia link to this file (pages on other projects are not listed):
- Talk:Albinism
- Talk:Down syndrome
- Talk:Asperger syndrome
- Talk:Marfan syndrome
- Talk:Gene therapy
- Talk:Color blindness
- Talk:Sickle-cell disease
- Talk:Crohn's disease
- Talk:Adducted thumb syndrome
- Talk:Polydactyly
- Talk:Gulf War syndrome
- Talk:Hereditary spastic paraplegia
- Talk:Klinefelter's syndrome
- Talk:Androgen insensitivity syndrome
- Talk:Familial Alzheimer disease
- Talk:Thalassemia
- Talk:Tourette syndrome
- Talk:Howel-Evans syndrome
- Talk:Coeliac disease
- Talk:Migraine
- Talk:Turner syndrome
- Talk:Brugada syndrome
- Talk:Huntington's disease
- Talk:Haemophilia
- Talk:Haemochromatosis
- Talk:Muscular dystrophy
- Talk:Harlequin type ichthyosis
- Talk:Ichthyosis
- Talk:Situs inversus
- Talk:Primary ciliary dyskinesia
- Talk:Alpha 1-antitrypsin deficiency
- Talk:Homocystinuria
- Talk:Fragile X syndrome
- Talk:Congenital adrenal hyperplasia
- Talk:Kabuki syndrome
- Talk:Photic sneeze reflex
- Talk:Medium-chain acyl-coenzyme A dehydrogenase deficiency
- Talk:Cystic fibrosis
- Talk:Cytogenetics
- Talk:Philadelphia chromosome
- Talk:Porphyria
- Talk:Ornithine transcarbamylase deficiency
- Talk:Aarskog syndrome
- Talk:Lesch-Nyhan syndrome
- Talk:Wolf-Hirschhorn syndrome
- Talk:Malignant hyperthermia
- Talk:Spina bifida
- Talk:List of genetic disorders
- Talk:Langer-Giedion syndrome
- Talk:Phenylketonuria
- Talk:Gaucher's disease
- Talk:Progeria
- Talk:Peutz-Jeghers syndrome
- Talk:Fructose intolerance
- Talk:Craniopagus parasiticus
- Talk:Aneuploidy
- Talk:Familial adenomatous polyposis
- Talk:Thanatophoric dysplasia
- Talk:Abetalipoproteinemia
- Talk:Retinitis pigmentosa
- Talk:Bardet-Biedl syndrome
- Talk:Tay-Sachs disease
- Talk:Ataxia telangiectasia
- Talk:Human genetic engineering
- Talk:Fabry's disease
- Talk:MOMO syndrome
- Talk:XYY syndrome
- Talk:Fructose malabsorption
- Talk:Williams syndrome
- Talk:Epidermolysis bullosa
- Talk:Adrenoleukodystrophy
- Talk:Spinocerebellar ataxia
- Talk:Leber's hereditary optic neuropathy
- Talk:ΔF508
- Talk:Gilbert's syndrome
- Talk:Angelman syndrome
- Talk:Genetic disorder
- Talk:Osteogenesis imperfecta
- Talk:Noonan syndrome
- Talk:Neurofibromatosis type II
- User:Jfurr1981
- Talk:Prader-Willi syndrome
- Talk:Sex linkage
- User:NCurse
- Talk:Aase syndrome
- Talk:Van Goethem syndrome
- Talk:Genetic testing
- Talk:Hurler syndrome
- Talk:Mucopolysaccharidosis
- Talk:Triple X syndrome
- Talk:Behr's syndrome
- Talk:Niemann-Pick disease
- Talk:Glycogen storage disease type II
- Talk:Copper toxicosis
- Talk:Lipid storage disorder
- Talk:Stickler syndrome
- Talk:Hypokalemic periodic paralysis
- Talk:Cavernous angioma
- Talk:Myotonia congenita
- Talk:Rett syndrome
- Talk:Hunter syndrome
- Talk:Edwards syndrome
- Talk:Nonsyndromic deafness
- Talk:Tetrahydrobiopterin deficiency
- Talk:Crouzonodermoskeletal syndrome
- Talk:Porphyria cutanea tarda
- Talk:Jackson-Weiss syndrome
- Talk:Pfeiffer syndrome
- Talk:Long QT syndrome
- Wikipedia:Userboxes/WikiProjects
- Talk:Argininosuccinic aciduria
- Talk:Patau syndrome
- Talk:Amelogenesis imperfecta
- Talk:Glutaric acidemia type 2
- Talk:Costello syndrome
- Talk:SADDAN
- Talk:Ascertainment bias
- Talk:Neurofibromatosis
- Talk:Genetic screen
- Talk:Neurofibromatosis type I
- Talk:Congenital adrenal hyperplasia due to 3 beta-hydroxysteroid dehydrogenase deficiency
- Talk:Genetic counseling
- Talk:Treacher Collins syndrome
- Talk:Hereditary hemorrhagic telangiectasia
- Talk:Facioscapulohumeral muscular dystrophy
- Talk:Cockayne syndrome
- Talk:Familial dysautonomia
- Talk:Werner syndrome
- Talk:Duchenne muscular dystrophy
- Talk:Phenylalanine hydroxylase
- Talk:3-Methylcrotonyl-CoA carboxylase deficiency
- Talk:Acrodermatitis enteropathica
- Talk:Joubert syndrome
- User:Leevanjackson
- Talk:Leigh's disease
- User:Apers0n
- Talk:Achondroplasia
- Talk:Haemophilia in European royalty
- Talk:Myopathy
- Talk:Tuberous sclerosis
- Talk:Charcot-Marie-Tooth disease
- Talk:Dor Yeshorim
- Talk:Laurence-Moon syndrome
- Talk:Robinow syndrome
- Talk:List of congenital disorders
- Talk:Smith-Magenis syndrome
- Talk:Cri du chat
- Talk:Wilson's disease
- Talk:Xeroderma pigmentosum
- Talk:CCR5
- Talk:Pallister-Killian syndrome
- Talk:XX male syndrome
- Talk:Microcephaly
- Talk:Androgenetic alopecia
- Talk:Galactosemia
- Wikipedia:WikiProject Medical Genetics
- Wikipedia:WikiProject Medical Genetics/Participants
- User:Apers0n/Temp
- Template:User WPMEDGENP1
- User:V0d4n
- Talk:22q13 deletion syndrome
- Talk:Nager syndrome
- Talk:22q11.2 deletion syndrome
- Talk:Kennedy disease
- Talk:Paramyotonia congenita
- Template:MedGen
- Talk:Anticipation (genetics)
- Talk:Medical genetics
- Talk:Mitochondrial disease
- Talk:X-linked dominant
- Talk:X-linked recessive
- Talk:Alexander disease
- Talk:Trinucleotide repeat disorders
- Talk:Canavan disease
- Talk:Spinal muscular atrophy
- Talk:Von Willebrand disease
- Talk:1p36 deletion syndrome
- Talk:2-Methylbutyryl-CoA dehydrogenase deficiency
- Talk:2,8 dihydroxy-adenine urolithiasis
- Talk:3-hydroxy-3-methylglutaryl-CoA lyase deficiency
- Talk:3-Methylglutaconic aciduria
- Talk:Health aspects of Down syndrome
- Talk:Multiple osteochondromatosis
- Talk:Hereditary multiple exostoses
- Talk:Dextrocardia
- Talk:Acute fatty liver of pregnancy
- Talk:49 XXXXY syndrome
- Talk:6-Pyruvoyltetrahydropterin synthase deficiency
- Talk:ALA dehydratase deficiency
- Talk:ZAP70 deficiency
- Talk:XX gonadal dysgenesis
- Talk:X-linked ichthyosis
- Talk:McCune-Albright syndrome
- Talk:X-linked adrenal hypoplasia congenita
- Talk:Wiskott-Aldrich syndrome
- Talk:Adenosine deaminase deficiency
- Talk:Leopard syndrome
- Talk:Kallmann syndrome
- Talk:Weissenbacher-Zweymüller syndrome
- Talk:Waardenburg syndrome
- Talk:Abderhalden-Kaufmann-Lignac syndrome
- Talk:Acatalasemia
- Talk:Aceruloplasminemia
- Talk:Accelerated aging disease
- Talk:Achondrogenesis
- Talk:WAGR syndrome
- Talk:Vitelliform macular dystrophy
- Talk:Very long-chain acyl-coenzyme A dehydrogenase deficiency
- Talk:Van der Woude syndrome
- Talk:Usher syndrome
- Talk:Tyrosinemia
- Talk:Turcot syndrome
- Talk:Trisomy 9
- Talk:Salla disease
- Talk:Simpson-Golabi-Behmel syndrome
- Talk:Spondyloperipheral dysplasia
- Talk:Thomsen disease
- Talk:Timothy syndrome
- Talk:Fetal Dilantin Syndrome
- Talk:Trimethylaminuria
- Talk:Thyroid hormone resistance
- Talk:Generalized epilepsy with febrile seizures plus
- Talk:Chronic granulomatous disease
- Talk:Tangier disease
- Talk:TAR syndrome
- Talk:Spondyloepiphyseal dysplasia congenita
- Talk:Spondyloepimetaphyseal dysplasia, Strudwick type
- Talk:Smith-Lemli-Opitz syndrome
- Talk:Adenylosuccinate lyase deficiency
- Talk:Shwachman-Diamond syndrome
- Talk:Sandhoff disease
- Talk:Rothmund-Thompson's syndrome
- Talk:Romano-Ward syndrome
- Talk:Short QT syndrome
- Talk:Recessive multiple epiphyseal dysplasia
- Talk:Propionic acidemia
- Talk:Progressive familial intrahepatic cholestasis
- Talk:Primary carnitine deficiency
- Talk:Acrofacial dysostosis, Nager type
- Talk:African iron overload
- Talk:Aicardi syndrome
- Talk:Alagille syndrome
- Talk:Alkaptonuria
- Talk:Popliteal pterygium syndrome
- Talk:Occipital horn syndrome
- Talk:Polychromia
- Talk:Preimplantation Genetic Haplotyping
- Talk:Preimplantation genetic diagnosis
- Talk:Alpha-mannosidosis
- Talk:Alport syndrome
- Talk:Alstrom syndrome
- Talk:Andersen-Tawil syndrome
- Talk:Apert syndrome
- Talk:Apparent mineralocorticoid excess
- Talk:Arakawa's syndrome II
- Talk:Atelosteogenesis, type II
- Talk:Bannayan-Zonana syndrome
- Talk:ATR-X
- Talk:Banti's syndrome
- Talk:Barth syndrome
- Talk:Bartter syndrome
- Talk:Becker's muscular dystrophy
- Talk:Beckwith-Wiedemann syndrome
- Talk:Berdon syndrome
- Talk:Beta-ketothiolase deficiency
- Talk:Biotinidase deficiency
- Talk:Birt-Hogg-Dubé syndrome
- Talk:Bloom syndrome
- Talk:Blue diaper syndrome
- Talk:Nail-patella syndrome
- Talk:Polycystic kidney disease
- Talk:Platyspondylic lethal skeletal dysplasia, Torrance type
- Talk:CADASIL
- Talk:Cystic fibrosis transmembrane conductance regulator
- Talk:Periodic paralysis
- Talk:Pendred syndrome
- Talk:Omenn syndrome
- Talk:Otospondylomegaepiphyseal dysplasia
- Talk:Pallister-Hall syndrome
- Talk:CDG syndrome
- Talk:Cardiofaciocutaneous syndrome
- Talk:Chromosome abnormalities
- Talk:Nullisomic
- Talk:Norrie disease
- Talk:Neonatal hemochromatosis
- Talk:Nemaline myopathy
- Talk:N-Acetylglutamate synthase deficiency
- Talk:Carnitine palmitoyltransferase I deficiency
- Talk:Carnitine palmitoyltransferase II deficiency
- Talk:Carnitine-acylcarnitine translocase deficiency
- Talk:Carpenter syndrome
- Talk:Channelopathy
- Talk:Fukuyama congenital muscular dystrophy
- Talk:Oculopharyngeal muscular dystrophy
- Talk:Chromosome 15q trisomy
- Talk:Chromosome 15q partial deletion
- Talk:Citrullinemia
- Talk:Myeloperoxidase deficiency
- Talk:Myelokathexis
- Talk:Multiple endocrine neoplasia type 2
- Talk:Multiple endocrine neoplasia type 1
- Talk:Mulibrey nanism
- Talk:Mitochondrial trifunctional protein deficiency
- Talk:Metachondromatosis
- Talk:MELAS
- Talk:Larsen syndrome
- Talk:Jervell and Lange-Nielsen syndrome
- Talk:Malonyl-CoA decarboxylase deficiency
- Talk:Kniest dysplasia
- Talk:Leukocyte adhesion deficiency
- Talk:Li-Fraumeni syndrome
- Talk:Lipoid congenital adrenal hyperplasia
- Talk:Ectrodactyly
- Talk:Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
- Talk:Lysinuric protein intolerance
- Talk:Maple syrup urine disease
- Talk:Coffin-Lowry syndrome
- Talk:Cohen syndrome
- Talk:Collagenopathy, types II and XI
- Talk:Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency
- Talk:Craniodiaphyseal dysplasia
- Talk:Crigler-Najjar syndrome
- Talk:Crouzon syndrome
- Talk:Cystinosis
- Talk:Cystinuria
- Talk:Dentinogenesis imperfecta
- Talk:Diamond-Blackfan anemia
- Talk:Diastrophic dysplasia
- Talk:Distal Trisomy 10q
- Talk:Duane-radial ray syndrome
- Talk:Ellis-van Creveld syndrome
- Talk:Emery-Dreifuss muscular dystrophy
- Talk:Engelmann syndrome
- Talk:Epidermolytic hyperkeratosis
- Talk:Congenital hyperinsulinism
- Talk:Familial Mediterranean fever
- Talk:Fanconi anemia
- Talk:Fraser syndrome
- Talk:GAPO syndrome
- Talk:GM2-gangliosidosis, AB variant
- Talk:Galloway Mowat syndrome
- Talk:Gitelman syndrome
- Talk:Glycogen storage disease type I
- Talk:Giant axonal neuropathy
- Talk:Glanzmann's thrombasthenia
- Talk:Glutaric acidemia type 1
- Talk:Glycogen storage disease type III
- Talk:Haemophilia C
- Talk:Hajdu-Cheney syndrome
- Talk:Greig cephalopolysyndactyly syndrome
- Talk:Haemophilia B
- Talk:Hereditary elliptocytosis
- Talk:Haemophilia A
- Talk:Hereditary nonpolyposis colorectal cancer
- Talk:Holocarboxylase synthetase deficiency
- Talk:Holt-Oram syndrome
- Talk:Hyperimmunoglobulinemia D with recurrent fever
- Talk:Hypochondrogenesis
- Talk:Hypochondroplasia
- Talk:Hyperkalemic periodic paralysis
- Talk:Ichthyosis vulgaris
- Talk:Infantile cortical hyperostosis
- Talk:Isovaleric acidemia
- Talk:Immunodeficiency, centromere instability and facial anomalies syndrome
- Talk:Impossible syndrome
- Talk:Incontinentia pigmenti
- Talk:4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency
- Talk:Acatalasia
- Talk:Achromatopsia
- Talk:Alternating hemiplegia of childhood
- Talk:Arginemia
- Talk:Asymmetric crying facies
- Talk:Asymptomatic carrier
- Talk:Autosomal dominant nocturnal frontal lobe epilepsy
- Talk:Bare lymphocyte syndrome
- Talk:Bare lymphocyte syndrome 2
- Talk:Benign familial neonatal convulsions
- Talk:Carbamoyl phosphate synthetase I deficiency
- Talk:Childhood absence epilepsy
- Talk:Chromosome instability syndrome
- Talk:Congenital muscular dystrophy
- Talk:Dystrophin
- Talk:Episodic Ataxia Type-1
- Talk:Erythromelalgia
- Talk:Ethylmalonic encephalopathy
- Talk:Factor IX
- Talk:Factor VIII
- Talk:Factor XI
- Talk:Familial amyloid polyneuropathy
- Talk:Familial hemiplegic migraine
- Talk:Flynn Aird syndrome
- Talk:Frontotemporal dementia and parkinsonism linked to chromosome 17
- Talk:Gardner's syndrome
- Talk:Genetic deletion
- Talk:Genetic origins of Down syndrome
- Talk:Hypohidrotic ectodermal dysplasia
- Talk:Hypomagnesemia with secondary hypocalcemia
- Talk:Isobutyryl-coenzyme A dehydrogenase deficiency
- Talk:Jacobsen syndrome
- Talk:Juvenile myoclonic epilepsy
- Talk:Kallman's Syndrome
- Talk:Kindler syndrome
- Talk:Krabbe disease
- Talk:Lethal white syndrome
- Talk:Liddle's Syndrome
- Talk:Loeys-Dietz syndrome
- Talk:Mammarial trisomy
- Talk:McLeod syndrome
- Talk:Metachromatic leukodystrophy
- Talk:Moonrise
- Talk:Myotonic dystrophy
- Talk:Nijmegen breakage syndrome
- Talk:Pelizaeus-Merzbacher disease
- Talk:Platyspondylic lethal skeletal dysplasia
- Talk:Progressive external ophthalmoplegia
- Talk:Pyruvate carboxylase deficiency
- Talk:Ring chromosome 20 syndrome
- Talk:Rubinstein-Taybi syndrome
- Talk:Schmitt Gillenwater Kelly syndrome
- Talk:Short-chain acyl-coenzyme A dehydrogenase deficiency
- Talk:Tylosis
- Talk:VACTERL association
- Talk:Von Hippel-Lindau disease
- Talk:Walker-Warburg syndrome
- Talk:X-linked alpha thalassemia mental retardation syndrome
- Talk:XXXX syndrome
- Talk:XXXXX syndrome
- Talk:Zellweger syndrome
- Talk:Isodicentric 15
- User:TheNewMessiah
- Talk:Kearns-Sayre syndrome
- Talk:MERRF syndrome
- Talk:Sideroblastic anemia
- Talk:Saethre-Chotzen syndrome
- Talk:PSI (prion)
- Talk:Wolfram syndrome
- Talk:List of genetic disorders-2