File:Autorecessive-es.svg
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Summary
DescriptionAutorecessive-es.svg |
English: Autosomal recessive gene Español: Gen autosómico recesivo. Modo de herencia entre dos portadores de un gen autosómico recesivo y monogénico. |
Date | |
Source | Own work in Inkscape |
Author | User:LordT modification from the original of en:User:Cburnett |
Permission (Reusing this file) |
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Items portrayed in this file
depicts
3 January 2007
image/svg+xml
d12b65dc5bf252ba398c060179c15be3a0cb8c13
40,327 byte
1,580 pixel
1,350 pixel
File history
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Date/Time | Thumbnail | Dimensions | User | Comment | |
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current | 17:28, 15 May 2014 | 1,350 × 1,580 (39 KB) | Basquetteur | corrijo mala traducción al español | |
15:29, 3 January 2008 | 1,350 × 1,580 (38 KB) | LordT | {{Information |Description={{en|Autosomal recessive gene}}{{es|Gen autosómica recesiva. Modo de herencia entre dos portadores de un gen autosómica recesiva y monogénica.}} |Source=Own work in Inkscape |Date=3 Jan [[2007 |
File usage
The following pages on the English Wikipedia use this file (pages on other projects are not listed):
Global file usage
The following other wikis use this file:
- Usage on ast.wikipedia.org
- Usage on es.wikipedia.org
- Ataxia de Friedreich
- Abetalipoproteinemia
- Fibrosis quística
- Enfermedad de Niemann-Pick
- Talasemia
- Enfermedad de Batten
- Anemia de células falciformes
- Mucopolisacaridosis
- Fenilcetonuria
- Anemia de Fanconi
- Beta-talasemia
- Enfermedad de Wilson
- Hemocromatosis hereditaria
- Ataxia-telangiectasia
- Síndrome de Hermansky-Pudlak
- Enfermedad de Tay-Sachs
- Autosoma
- Enfermedad de Farber
- Enfermedad de Krabbe
- Enfermedad de Gaucher
- Enfermedad de Canavan
- Síndrome de Cockayne
- Distrofia muscular congénita con déficit de merosina
- Galactosemia
- Enfermedad de Von Gierke
- Enfermedad de McArdle
- Enfermedad por almacenamiento de glucógeno tipo VII
- Síndrome de Allgrove
- Enfermedad poliquística renal
- Xerodermia pigmentosa
- Enfermedad de Von Willebrand
- Trombastenia de Glanzman
- Amaurosis congénita de Leber
- Deficiencia de holocarboxilasa sintetasa
- Síndrome de Waardenburg
- Abiotrofia cerebelosa
- Enfermedad de Pompe
- Síndrome de Ochoa
- Síndrome de Dubin-Johnson
- Síndrome de Papillon-Lefèvre
- Enfermedad de Hartnup
- Síndrome de Omenn
- Alcaptonuria
- Colestasis linfedema
- Síndrome de Sanfilippo
- Acatalasemia
- Fiebre mediterránea familiar
- Distrofia muscular de Emery-Dreifuss
View more global usage of this file.
Metadata
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Height | 1580 |
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