French
DeutschFile:X-linked dominant.svg
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Summary
| Description | English: X-linked dominant inheritance scenarios for either the mother or father being affected |
| Date | |
| Source | Based off of File:Autosomal dominant - 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 |
| Other versions |
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Licensing
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
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- 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.
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File history
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| Date/Time | Thumbnail | Dimensions | User | Comment | |
|---|---|---|---|---|---|
| current | 17:19, 21 January 2020 | | 1,525 × 1,283 (166 KB) | SUM1 | Vertically aligned legend boxes |
| 17:09, 21 January 2020 |  | 1,525 × 1,283 (166 KB) | SUM1 | User created page with UploadWizard |
File usage
The following 18 pages use this file:
- Bazex–Dupré–Christol syndrome
- Chromosome abnormality
- Coffin–Lowry syndrome
- Craniofrontonasal dysplasia
- List of conditions with craniosynostosis
- Lujan–Fryns syndrome
- Microphthalmia–dermal aplasia–sclerocornea syndrome
- Nance–Horan syndrome
- Phosphate diabetes
- Terminal osseous dysplasia with pigmentary defects
- X-linked cone-rod dystrophy, type 1
- X-linked dominant inheritance
- X-linked hypertrichosis
- X-linked hypophosphatemia
- User:Ilubphysics/sandbox
- User:SUM1/Contributions
- User:Saturnnebula
- User talk:Ozzie10aaaa
Global file usage
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- Usage on ar.wikipedia.org
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- Usage on fa.wikipedia.org
- Usage on he.wikipedia.org
- Usage on it.wikipedia.org
- Usage on mk.wikipedia.org
- Usage on zh.wikipedia.org
