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File:Chromosome.svg
From WikiMD's Food, Medicine & Wellness Encyclopedia
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Original file (SVG file, nominally 688 × 848 pixels, file size: 29 KB)
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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.
- 15q11.2 microdeletion
- 49,XYYYY
- 6-Pyruvoyltetrahydropterin synthase deficiency
- Abdallat–Davis–Farrage syndrome
- Abruzzo–Erickson syndrome
- Acheiropodia
- Achondrogenesis type 1B
- Acrofrontofacionasal dysostosis
- Acrofrontofacionasal dysostosis syndrome
- Acromesomelic dysplasia
- Aldosterone synthase deficiency
- Aldred syndrome
- Alopecia contractures dwarfism mental retardation
- Alopecia contractures dwarfism mental retardation syndrome
- Aminolevulinic acid dehydratase deficiency porphyria
- Angel-shaped phalango-epiphyseal dysplasia
- Ataxia with vitamin E deficiency
- Axenfeld syndrome
- Becker disease
- Benign hereditary chorea
- Beta thalassemia
- Bifid penis
- Bilateral renal agenesis dominant type
- Bjornstad syndrome
- Blepharonasofacial malformation syndrome
- Bone fragility craniosynostosis proptosis hydrocephalus
- Bourneville's disease
- Brain-lung-thyroid syndrome
- Centromere
- Chediak-higashi syndrome
- Cholemia
- Chondrodysplasia punctata
- Chromatid
- Chromosome 15q duplication
- Chromosome 2q deletion
- Chylomicron retention disease
- Cleidocranial
- Collagenopathy, types II and XI
- Complement 4 deficiency
- Congenital disorder of glycosylation type IIc
- Congenital ichthyosiform erythroderma
- Congenital myasthenic syndrome
- Desmin-related myofibrillar myopathy
- Dilated cardiomyopathy with hypergonadotropic hypogonadism
- Distal spinal muscular atrophy type 2
- Dunnigan familial partial lipodystrophy
- Erythrokeratodermia variabilis et progressiva
- Familial HDL deficiency
- Follicular ichthyosis
- GRACILE syndrome
- Gamma-cystathionase deficiency
- Glycogen storage disease type iv
- Goldberg-Shprintzen megacolon syndrome
- Gonadotropin-releasing hormone insensitivity
- Gonadotropin insensitivity
- Hemochromatosis type 3
- Hereditary gingival fibromatosis
- Hereditary motor and sensory neuropathy with proximal dominance
- Hereditary mucoepithelial dysplasia
- Hereditary spherocytosis 1
- ICF syndrome
- Inherited disorders of trafficking
- Jokela type spinal muscular atrophy
- Kufs disease
- Lateral meningocele syndrome
- MODY 5
- Megalencephalic leukoencephalopathy with subcortical cysts
- Metachondromatosis
- Microorchidism
- Mohr–Tranebjærg syndrome
- Monilethrix
- Mucolipidosis type IV
- Oculocutaneous albinism type I
- Orofaciodigital syndrome 2
- Paris-Trousseau thrombocytopenia
- Parkinson disease type 9
- Popliteal pterygium
- Prader-Willi habitus, osteopenia, and camptodactyly
- Pure hair-nail type ectodermal dysplasia
- Renal-hepatic-pancreatic dysplasia
- Ring chromosome 20
- SLC35C1-CDG (CDG-IIc)
- Saccharopinuria
- Senior Loken Syndrome
- Short rib-polydactyly syndrome 3
- Singleton-Merten syndrome
- Spastic ataxia-corneal dystrophy syndrome
- Spinal muscular atrophy with lower extremity predominance
- Spinal muscular atrophy with progressive myoclonic epilepsy
- Sprengel deformity
- Sucrose intolerance
- Syndrome of apparent mineralocorticoid excess
- Terminal complement pathway deficiency
- Trisomy 10
- WNT4 deficiency
- Wiedemann–Rautenstrauch syndrome
- X-linked spinal muscular atrophy type 2
- Yim–Ebbin syndrome
- Zamzam–Sheriff–Phillips syndrome
- Zechi-Ceide syndrome
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