File:X-linked recessive (2).svg
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Summary
| Description |
English: X-linked recessive inheritance scenarios for either the mother being a carrier or the father being affected |
| Date | |
| 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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| Other versions |
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Licensing
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File history
Click on a date/time to view the file as it appeared at that time.
| Date/Time | Thumbnail | Dimensions | User | Comment | |
|---|---|---|---|---|---|
| current | 04:51, 21 January 2020 | | 1,525 × 1,283 (169 KB) | SUM1 | Switched carrier mother children to be more centred |
| 03:57, 21 January 2020 |  | 1,525 × 1,283 (170 KB) | SUM1 | User created page with UploadWizard |
File usage
The following 19 pages use this file:
- Gustavson syndrome
- Haemophilia
- Haemophilia B
- Hypohidrotic ectodermal dysplasia with immune deficiency
- Keratosis follicularis-dwarfism-cerebral atrophy syndrome
- Morse–Rawnsley–Sargent syndrome
- Pierre Robin sequence-faciodigital anomaly syndrome
- Retinoschisis
- Rud syndrome
- Spinal and bulbar muscular atrophy
- Stocco dos Santos syndrome
- Tranebjaerg–Svejgaard syndrome
- X-linked complicated corpus callosum dysgenesis
- X-linked genetic disease
- X-linked recessive hypoparathyroidism
- X-linked recessive inheritance
- X-linked severe combined immunodeficiency
- User:SUM1/Contributions
- User talk:Ozzie10aaaa
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