File:X-linked dominant.svg
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Summary
[edit]| 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
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.svg){kind=small}
.svg){kind=small}
Licensing
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This file is licensed under the Creative Commons Attribution-Share Alike 4.0 International license.
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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 (talk | contribs) | Vertically aligned legend boxes |
| 17:09, 21 January 2020 |  | 1,525 × 1,283 (166 KB) | SUM1 (talk | contribs) | User created page with UploadWizard |
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File usage on Commons
The following 2 pages use this file:
File usage on other wikis
The following other wikis use this file:
- Usage on ar.wikipedia.org
- Usage on bs.wikipedia.org
- Usage on en.wikipedia.org
- Coffin–Lowry syndrome
- X-linked dominant inheritance
- X-linked hypophosphatemia
- Craniofrontonasal dysplasia
- Bazex–Dupré–Christol syndrome
- Lujan–Fryns syndrome
- X-linked hypertrichosis
- Terminal osseous dysplasia with pigmentary defects
- Microphthalmia–dermal aplasia–sclerocornea syndrome
- User talk:Ozzie10aaaa
- Nance–Horan syndrome
- User:SUM1/Contributions
- HNRNPH2-related disorders
- X-linked cone-rod dystrophy, type 1
- User:Ilubphysics/sandbox
- User:Saturnnebula
- Phosphate diabetes
- List of conditions with craniosynostosis
- Usage on es.wikipedia.org
- Usage on fa.wikipedia.org
- Usage on he.wikipedia.org
- Usage on it.wikipedia.org
- Usage on zh.wikipedia.org
