![File:Chromosome.svg](https://upload.wikimedia.org/wikipedia/commons/thumb/0/0b/Chromosome.svg/486px-Chromosome.svg.png)
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Date/Time | Thumbnail | Dimensions | User | Comment | |
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current | 05:59, 27 July 2022 | ![]() | 688 × 848 (29 KB) | Glrx | fix W3 error |
05:53, 27 July 2022 | ![]() | 688 × 848 (29 KB) | Glrx | workaround librsvg bug | |
05:49, 27 July 2022 | ![]() | 688 × 848 (29 KB) | Glrx | restore original. remove path text. convert curves to text | |
13:55, 26 November 2008 | ![]() | 688 × 848 (42 KB) | Tryphon | Converted font to path, as it didn't seem to work in Firefox 3. | |
13:52, 26 November 2008 | ![]() | 688 × 848 (40 KB) | Tryphon | {{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 arm. |
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- Acrofrontofacionasal dysostosis
- Acytosiosis
- Alopecia contractures dwarfism intellectual disability syndrome
- Amazia
- Aniridia renal agenesis psychomotor retardation
- Asymmetric crying facies
- Athelia (disease)
- Ayazi syndrome
- Bamforth–Lazarus syndrome
- Benjamin syndrome
- Berk–Tabatznik syndrome
- Biemond syndrome
- Bifid penis
- Calciumopathy
- Centromere
- Chromatid
- Chromosome
- Chromosome 15q partial deletion
- Congenital disorder of glycosylation type IIc
- Congenital fibrosis of the extraocular muscles
- Erondu–Cymet syndrome
- Erythrokeratodermia variabilis
- FACES syndrome
- Familial cirrhosis
- Familial male-limited precocious puberty
- Familial renal amyloidosis
- First arch syndrome
- Fleck corneal dystrophy
- Fleischer's syndrome
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- Halal syndrome
- Hawkinsinuria
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- Ho–Kaufman–Mcalister syndrome
- Hurler–Scheie syndrome
- Hypoalphalipoproteinemia
- Hypoplasminogenemia
- Inherited disorders of trafficking
- Johnson–Munson syndrome
- Keppen–Lubinsky syndrome
- Lachiewicz–Sibley syndrome
- Lisch epithelial corneal dystrophy
- Locus (genetics)
- Lucey–Driscoll syndrome
- Majewski's polydactyly syndrome
- McKusick–Kaufman syndrome
- Meige disease
- Metaphyseal chondrodysplasia Schmid type
- Michels syndrome
- Microcephalic osteodysplastic primordial dwarfism type II
- Microcheilia
- Microorchidism
- Molecular models of DNA
- Monosomy 14
- Multiple abnormalities
- Mungan syndrome
- Musculoskeletal abnormality
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- Neonatal adrenoleukodystrophy
- Neutrophil immunodeficiency syndrome
- Njølstad syndrome
- Norman–Roberts syndrome
- Nullisomic
- Orofaciodigital syndrome
- Pacman dysplasia
- Palmoplantar ectodermal dysplasia
- Paris-Trousseau syndrome
- Partial monosomy 13q
- Pashayan syndrome
- Patterson syndrome
- Pilotto syndrome
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- Polysplenia
- Pure hair-nail type ectodermal dysplasia
- Ramos-Arroyo syndrome
- Reynolds syndrome
- Rudiger syndrome
- Saal Bulas syndrome
- Saccharopinuria
- Seaver–Cassidy syndrome
- Smith–Martin–Dodd syndrome
- Status marmoratus
- Stratton Parker syndrome
- Sugarman syndrome
- Synpolydactyly
- Teunissen–Cremers syndrome
- Urban–Rogers–Meyer syndrome
- VLDLR-associated cerebellar hypoplasia
- Warkany syndrome 1
- X-linked endothelial corneal dystrophy
- Zamzam–Sheriff–Phillips syndrome
- Zonular cataract and nystagmus
- Zori–Stalker–Williams syndrome
- Talk:Molecular models of DNA/Galleries
- User:Bci2
- User:Bci2/Books/Wk2Book
- User:Bci2/Books/Wk3vol1
- User:Bci2/Books/Wk4
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