File:X-linked recessive (2).svg
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Size of this PNG preview of this SVG file: 713 × 600 pixels. Other resolutions: 285 × 240 pixels | 571 × 480 pixels | 913 × 768 pixels | 1,217 × 1,024 pixels | 2,434 × 2,048 pixels | 1,525 × 1,283 pixels.
Original file (SVG file, nominally 1,525 × 1,283 pixels, file size: 169 KB)
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Summary[edit]
| Description |
English: X-linked recessive inheritance scenarios for either the mother being a carrier or the father being affected |
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| Source | Based off of File:Autosomal recessive - en.svg |
| Author |
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| Note | For use on syndromes in which an affected male might be expected to pass on the condition. If not, use
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Licensing[edit]
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This file is licensed under the Creative Commons Attribution-Share Alike 4.0 International license.
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- to share – to copy, distribute and transmit the work
- to remix – to adapt the work
- Under the following conditions:
- attribution – You must give appropriate credit, provide a link to the license, and indicate if changes were made. You may do so in any reasonable manner, but not in any way that suggests the licensor endorses you or your use.
- share alike – If you remix, transform, or build upon the material, you must distribute your contributions under the same or compatible license as the original.
File history
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| Date/Time | Thumbnail | Dimensions | User | Comment | |
|---|---|---|---|---|---|
| current | 04:51, 21 January 2020 | | 1,525 × 1,283 (169 KB) | SUM1 (talk | contribs) | Switched carrier mother children to be more centred |
| 03:57, 21 January 2020 |  | 1,525 × 1,283 (170 KB) | SUM1 (talk | contribs) | User created page with UploadWizard |
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File usage on Commons
The following 3 pages use this file:
File usage on other wikis
The following other wikis use this file:
- Usage on bs.wikipedia.org
- Usage on el.wikipedia.org
- Usage on en.wikipedia.org
- Haemophilia
- Haemophilia B
- Retinoschisis
- X-linked recessive inheritance
- Spinal and bulbar muscular atrophy
- X-linked severe combined immunodeficiency
- Pattern hair loss
- Rud syndrome
- User talk:Ozzie10aaaa
- X-linked recessive hypoparathyroidism
- User:SUM1/Contributions
- Stocco dos Santos syndrome
- Morse–Rawnsley–Sargent syndrome
- Gustavson syndrome
- Tranebjaerg–Svejgaard syndrome
- Pierre Robin sequence-faciodigital anomaly syndrome
- X-linked complicated corpus callosum dysgenesis
- Hypohidrotic ectodermal dysplasia with immune deficiency
- Keratosis follicularis-dwarfism-cerebral atrophy syndrome
- User:HuangWendi/X-linked Genetic Disease
- Usage on ga.wikipedia.org
- Usage on he.wikipedia.org
- Usage on it.wikipedia.org
- Usage on ja.wikipedia.org
- Usage on zh.wikipedia.org
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