File:X-linked recessive.svg
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![File:X-linked recessive.svg](http://upload.wikimedia.org/wikipedia/commons/thumb/c/c7/X-linked_recessive.svg/395px-X-linked_recessive.svg.png)
Size of this PNG preview of this SVG file: 395 × 600 pixels. Other resolutions: 158 × 240 pixels | 316 × 480 pixels | 506 × 768 pixels | 674 × 1,024 pixels | 1,349 × 2,048 pixels | 600 × 911 pixels.
Original file (SVG file, nominally 600 × 911 pixels, file size: 136 KB)
File history
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Date/Time | Thumbnail | Dimensions | User | Comment | |
---|---|---|---|---|---|
current | 23:52, 27 November 2014 | ![]() | 600 × 911 (136 KB) | Kashmiri | Minor colour corrections |
23:37, 27 November 2014 | ![]() | 600 × 911 (129 KB) | Kashmiri | Minor corrections | |
23:26, 27 November 2014 | ![]() | 601 × 912 (129 KB) | Kashmiri | Description added as per original source image; layout improvements | |
02:22, 14 November 2010 | ![]() | 765 × 990 (79 KB) | Drsrisenthil | {{Information |Description=X-linked Recessive inheritance From http://ghr.nlm.nih.gov/ *Re-creation of entire image in svg format by drsrisenthil |Source=*File:XlinkRecessive.jpg |Date=2010-11-14 02:14 (UTC) |Author=*File:XlinkRecessive.jpg: |
File usage
The following pages on the English Wikipedia use this file (pages on other projects are not listed):
- Aarskog–Scott syndrome
- Albinism–deafness syndrome
- Allan–Herndon–Dudley syndrome
- Arts syndrome
- Ayazi syndrome
- Becker muscular dystrophy
- David Gardner-Medwin
- Dent's disease
- Duchenne muscular dystrophy
- Dyskeratosis congenita
- Hoyeraal–Hreidarsson syndrome
- Hunter syndrome
- Hyper-IgM syndrome type 1
- Hypohidrotic ectodermal dysplasia
- IPEX syndrome
- Ichthyosis follicularis with alopecia and photophobia syndrome
- Immunodeficiency with hyperimmunoglobulin M
- L1 syndrome
- Lesch–Nyhan syndrome
- Lisch epithelial corneal dystrophy
- McLeod syndrome
- Mohr–Tranebjærg syndrome
- Morgagni–Stewart–Morel syndrome
- Myopathy, X-linked, with excessive autophagy
- Nasodigitoacoustic syndrome
- Norrie disease
- Ocular albinism type 1
- Oculocerebrorenal syndrome
- Properdin deficiency
- Renpenning's syndrome
- SCARF syndrome
- Simpson–Golabi–Behmel syndrome
- Smith–Fineman–Myers syndrome
- Wieacker syndrome
- Wiskott–Aldrich syndrome
- X-linked agammaglobulinemia
- X-linked dystonia parkinsonism
- X-linked ichthyosis
- X-linked myotubular myopathy
- X-linked spinal muscular atrophy type 2
- X-linked thrombocytopenia
- XMEN disease
- User:Iolejniczak/sandbox
- User:Ozzie10aaaa/med edit/lab
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