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Size of this preview: 345 × 600 pixels. Other resolutions: 138 × 240 pixels | 276 × 480 pixels. Full resolution ‎(SVG file, nominally 738 × 1,283 pixels, file size: 165 KB) This image rendered as PNG in other sizes: 200px, 500px, 1000px, 2000px.

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Summary[edit]

Description

English: Autosomal dominant - genetics (ESPAÑOL version) Français : Transmission autosomique dominante avec un parent porteur (version anglaise)

Date 3 March 2012

Source

English: Own work based on File:ABO system codominance.svg and File:Autodominant.jpg Français : Own work basé sur File:ABO system codominance.svg et File:Autodominant.jpg

Author

Français : Domaina

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Derivative works of this file: Autosomal dominant - de.svgFile:Autosomal dominant - fr.svg

Licensing[edit]

I, the copyright holder of this work, hereby publish it under the following license:

This file is licensed under the Creative Commons Attribution-Share Alike 3.0 Unported license.

You are free: to share – to copy, distribute and transmit the work to remix – to adapt the work Under the following conditions: attribution – You must attribute the work in the manner specified by the author or licensor (but not in any way that suggests that they endorse you or your use of the work). share alike – If you alter, transform, or build upon this work, you may distribute the resulting work only under the same or similar license to this one.

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11:36, 3 March 2012

738 × 1,283 (165 KB)

Domaina

File usage

The following pages on the English Wikipedia link to this file (pages on other projects are not listed): Acropectoral syndrome Albright's hereditary osteodystrophy Arakawa's syndrome II Autosomal dominant cerebellar ataxia Axenfeld syndrome Bethlem myopathy Birt–Hogg–Dubé syndrome Boomerang dysplasia Branchio-oto-renal syndrome Buschke–Ollendorff syndrome Central core disease Congenital stromal corneal dystrophy Currarino syndrome Darier's disease De Vivo disease Dermatopathia pigmentosa reticularis DiGeorge syndrome Dominance (genetics) Familial atrial fibrillation Familial male-limited precocious puberty Feingold syndrome Flynn–Aird syndrome Gardner's syndrome Greig cephalopolysyndactyly syndrome Hajdu–Cheney syndrome Hawkinsinuria Hay–Wells syndrome Hereditary hemorrhagic telangiectasia Hereditary sensory and autonomic neuropathy type I Holt–Oram syndrome Human genetics Hypoalphalipoproteinemia Jackson–Weiss syndrome Keratolytic winter erythema Kniest dysplasia Kostmann syndrome Liddle's syndrome MOMO syndrome Marshall syndrome Medullary cystic kidney disease Metachondromatosis Monilethrix Multiple endocrine neoplasia type 2 Myotonic dystrophy Naegeli–Franceschetti–Jadassohn syndrome Nail–patella syndrome Noonan syndrome PAPA syndrome Pachyonychia congenita Pallister–Hall syndrome Papillorenal syndrome Pelger-Huet anomaly Platyspondylic lethal skeletal dysplasia, Torrance type Popliteal pterygium syndrome Porphyria cutanea tarda Romano–Ward syndrome Rubinstein–Taybi syndrome Schmitt Gillenwater Kelly syndrome Short QT syndrome Spinocerebellar ataxia Spondyloepimetaphyseal dysplasia, Strudwick type Spondyloperipheral dysplasia Steatocystoma multiplex Stickler syndrome Tietz syndrome Timothy syndrome Transthyretin-related hereditary amyloidosis Treacher Collins syndrome Triangular alopecia Tuberous sclerosis Upington disease Variegate porphyria Vitelliform macular dystrophy Von Hippel–Lindau disease Von Willebrand disease WHIM syndrome Waardenburg syndrome Wallis–Zieff–Goldblatt syndrome White sponge nevus Worth syndrome Zaspopathy Zimmermann–Laband syndrome Zori–Stalker–Williams syndrome User:Augustinus Galih/sandbox Global file usage

The following other wikis use this file: Usage on bg.wikipedia.org Спиноцеребеларна атаксия Usage on cs.wikipedia.org Larsenův syndrom Usage on fr.wikipedia.org Syndrome MOMO Usage on gl.wikipedia.org Dominancia (xenética) Usage on hu.wikipedia.org Von Willebrand-Jürgens szindróma

Metadata This file contains additional information, probably added from the digital camera or scanner used to create or digitize it. If the file has been modified from its original state, some details may not fully reflect the modified file.

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