Image:Chromosome-upright.png
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Chromosome-upright.png (200 × 287 pixels, file size: 7 KB, MIME type: image/png)
| This is a file from the Wikimedia Commons. The description on its description page there is shown below.
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| Description |
English: Scheme of a Chromosome. (1) Chromatid. One of the two identical parts of the chromosome after S phase. (2) Centromere. The point where the two chromatids touch, and where the microtubules attach. (3) Short arm (4) Long arm. In accordance with the display rules in Cytogenetics, the short arm is on top.
Deutsch: Schema eines Chromosoms: 1. Chromatid, 2. Centromer (auch Spindelfaseransatzstelle genannt), der Punkt, an dem sich die beiden Chromatiden berühren, 3. Kurzer Arm. (p-Arm), 4. Langer Arm. (q-Arm). Entsprechend der üblichen Darstellung in der Cytogenetik ist der kurze Arm oben, der lange unten.
日本語: 染色体: (1) 染色分体:染色体に含まれる2つの同一の部分のうちの片方 (2) セントロメア: 2つの染色分体が接合する場所で、ここに微小管が結合する (3) 短腕 (4) 長腕
Nederlands: Afb. 1. Chromosoom: 1. Chromatide, 2. Centromeer, 3. Korte arm, 4. Lange arm
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| Source |
Nupedia, then en.wikipedia |
| Date |
Original version uploaded on en.wikipedia 21:18, October 4, 2002. This version: 7. March 2007 |
| Author |
Original version: Magnus Manske, this version with upright chromosome: User:Dietzel65 |
| Permission (Reusing this image) |
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| Other versions | This original version is "upside down". In Cytogenetics, chromosomes are always displayed with the short arm on top.:  |
File history
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| Date/Time | Dimensions | User | Comment | |
|---|---|---|---|---|
| current | 14:48, 7 March 2007 | 200×287 (7 KB) | Dietzel65 | ({{Information| |Description= {{en|Scheme of a Chromosome. (1) Chromatid. One of the two identical parts of the chromosome after S phase. (2) Centromere. The point where the two chromatids touch, and where the microtubules attach. (3) Short arm (4) Long ar) |
File links
The following pages on the English Wikipedia link to this file (pages on other projects are not listed):
- Chromosome
- Lafora disease
- Chromosome 15q trisomy
- Chromosome 15q partial deletion
- Brachydactyly
- Cenani Lenz syndactylism
- Say Meyer syndrome
- Warkany syndrome 2
- Acheiropodia
- Adducted thumb syndrome
- Congenital disorder of glycosylation
- Langer-Giedion syndrome
- Anotia
- Weissenbacher-Zweymüller syndrome
- Schmitt Gillenwater Kelly syndrome
- Sabinas brittle hair syndrome
- Acrofacial dysostosis, Nager type
- Occipital horn syndrome
- Haemophilia C
- ALA dehydratase deficiency
- Erythropoietic protoporphyria
- Methylmalonic acidemia
- Propionic acidemia
- Dextrocardia
- Adenosine deaminase deficiency
- Craniodiaphyseal dysplasia
- Hereditary fructose intolerance
- Beckwith-Wiedemann syndrome
- Cerebellar hypoplasia
- MASA syndrome
- Miller-Dieker syndrome
- Gardner's syndrome
- Alpha-mannosidosis
- Darier's disease
- Phosphofructokinase deficiency
- Oculopharyngeal muscular dystrophy
- Arachnodactyly
- Gunther's disease
- ICF syndrome
- Berdon syndrome
- Incontinentia pigmenti
- Myeloperoxidase deficiency
- Chromosome 5q deletion syndrome
- Turcot syndrome
- Fukuyama congenital muscular dystrophy
- Abderhalden-Kaufmann-Lignac syndrome
- Mulibrey nanism
- Van der Woude syndrome
- Myelokathexis
- Channelopathy
- Kostmann syndrome
- Saccharopinuria
- Salla disease
- Mitochondrial trifunctional protein deficiency
- Spondyloperipheral dysplasia
- Sideroblastic anemia
- Carpenter syndrome
- Dubin-Johnson syndrome
- Trisomy 9
- Metachondromatosis
- Glycogen storage disease type IV
- Glycogen storage disease type III
- Nullisomic
- Kearns-Sayre syndrome
- Hyperlysinemia
- ABCD syndrome
- Abdallat Davis Farrage syndrome
- Acatalasemia
- Van Goethem syndrome
- Behr's syndrome
- Thomsen disease
- Walker-Warburg syndrome
- Aceruloplasminemia
- African iron overload
- Nijmegen breakage syndrome
- Asymmetric crying facies
- Blue diaper syndrome
- Fountain syndrome
- ZAP70 deficiency
- Neonatal hemochromatosis
- Impossible syndrome
- Syndrome of Apparent Mineralocorticoid Excess
- Adenine phosphoribosyltransferase deficiency
- Malonyl-CoA decarboxylase deficiency
- 6-Pyruvoyltetrahydropterin synthase deficiency
- Short-chain acyl-coenzyme A dehydrogenase deficiency
- 2,4 Dienoyl-CoA reductase deficiency
- Flynn-Aird syndrome
- Liddle's syndrome
- GAPO syndrome
- Simpson-Golabi-Behmel syndrome
- Recessive multiple epiphyseal dysplasia
- Arakawa's syndrome II
- Galloway Mowat syndrome
- Triple A syndrome
- Hawkinsinuria
- Hajdu-Cheney syndrome
- Griscelli syndrome
- XXYY syndrome
- Rotor syndrome
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