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| current | 15:01, 30 January 2008 |  | 307 × 396 (66 KB) | Swilliams (talk | contribs) |
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File usage
The following file is a duplicate of this file (more details):
The following 24 pages use this file:
- 22q11.2 deletion syndrome pathophysiology
- Branchio-oto-renal syndrome
- Central core disease
- Familial atrial fibrillation
- Gardner's syndrome
- Greig cephalopolysyndactyly syndrome
- Hawkinsinuria
- Larsen syndrome
- Myotonic dystrophy
- Pachyonychia congenita
- Pelger-Huet anomaly
- Popliteal pterygium syndrome
- Porphyria cutanea tarda causes
- Saethre-Chotzen syndrome
- Spinocerebellar ataxia
- Spondyloepiphyseal dysplasia congenita
- Vitelliform macular dystrophy
- Von Willebrand disease pathophysiology
- WHIM syndrome
- Wallis Zieff Goldblatt syndrome
- White sponge nevus
- Zaspopathy
- Zimmerman-Laband syndrome
- Zori Stalker Williams syndrome
