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File:Chromosome.svg
From WikiMD's Food, Medicine & Wellness Encyclopedia
Size of this PNG preview of this SVG file: 486 × 599 pixels. Other resolution: 1,661 × 2,048 pixels.
Original file (SVG file, nominally 688 × 848 pixels, file size: 29 KB)
File history
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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 |
File usage
The following file is a duplicate of this file (more details):
- File:Chromosome.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.
- 6-Pyruvoyltetrahydropterin synthase deficiency
- Abdallat–Davis–Farrage syndrome
- Abruzzo–Erickson syndrome
- Acheiropodia
- Acrofrontofacionasal dysostosis
- Acromesomelic dysplasia
- Aldosterone synthase deficiency
- Aldred syndrome
- Alopecia contractures dwarfism mental retardation syndrome
- Benign hereditary chorea
- Bifid penis
- Bjornstad syndrome
- Centromere
- Chediak-higashi syndrome
- Cholemia
- Chondrodysplasia punctata
- Chromatid
- Chromosome 2q deletion
- Congenital disorder of glycosylation type IIc
- Distal spinal muscular atrophy type 2
- EAST syndrome
- Enamel-renal syndrome
- GM2-gangliosidosis, AB variant
- GRACILE syndrome
- Gonadotropin-releasing hormone insensitivity
- Hagemoser–Weinstein–Bresnick syndrome
- Hailey–Hailey disease
- Hereditary motor and sensory neuropathy with proximal dominance
- Hereditary mucoepithelial dysplasia
- ICF syndrome
- Immunodeficiency–centromeric instability–facial anomalies syndrome
- Inherited disorders of trafficking
- Jokela type spinal muscular atrophy
- Katz syndrome
- Kosaki overgrowth syndrome
- L1 syndrome
- Larsen syndrome
- Lateral meningocele syndrome
- Lucey–Driscoll syndrome
- MECP2 duplication syndrome
- MORM syndrome
- Mahvash disease
- Marshall syndrome
- McGillivray syndrome
- Megalencephalic leukoencephalopathy with subcortical cysts
- Meleda disease
- Metachondromatosis
- Michels syndrome
- Microorchidism
- Mohr–Tranebjærg syndrome
- Monilethrix
- Multicentric carpotarsal osteolysis syndrome
- Myopathy, X-linked, with excessive autophagy
- Naegeli–Franceschetti–Jadassohn syndrome
- Norrie disease
- Occipital horn syndrome
- Oculocutaneous albinism type I
- Oculofaciocardiodental syndrome
- Orofaciodigital syndrome 1
- PLAID syndrome
- Pashayan syndrome
- Pure hair-nail type ectodermal dysplasia
- Ramos-Arroyo syndrome
- Renal-hepatic-pancreatic dysplasia
- Renal dysplasia-limb defects syndrome
- Revesz syndrome
- Ring chromosome 14 syndrome
- Ring chromosome 20
- Ring chromosome 20 syndrome
- Roberts syndrome
- Rombo syndrome
- Rothmund–Thomson syndrome
- Rudiger syndrome
- SCARF syndrome
- STAR syndrome
- Saccharopinuria
- Say syndrome
- Schmitt Gillenwater Kelly syndrome
- Schwartz–Jampel syndrome
- Sengers syndrome
- Senior–Løken syndrome
- Smith–Lemli–Opitz syndrome
- Spastic ataxia-corneal dystrophy syndrome
- Spinal muscular atrophy with lower extremity predominance
- Spinal muscular atrophy with progressive myoclonic epilepsy
- Stimmler syndrome
- Syndrome of apparent mineralocorticoid excess
- TAR syndrome
- TRIANGLE disease
- Tay–Sachs disease
- Terminal complement pathway deficiency
- Timothy syndrome
- Trichothiodystrophy
- Upington disease
- Urban–Rogers–Meyer syndrome
- WNT4 deficiency
- Wiedemann–Rautenstrauch syndrome
- X-linked spinal muscular atrophy type 2
- Yim–Ebbin syndrome
- Zamzam–Sheriff–Phillips syndrome
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