Generalized enchondromatosis in a boy with only platyspondyly in the father
β Scribed by Halal, Fahed ;Azouz, E. Michel
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- English
- Weight
- 443 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0148-7299
No coin nor oath required. For personal study only.
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SUMMARY: Walker Brown was born with a genetic mutation so rare that doctors call it an orphan syndrome: perhaps 300 people around the world also live with it. Walker turns twelve in 2008, but he weighs only 54 pounds, is still in diapers, can't speak and needs to wear special cuffs on his arms so th
SUMMARY: Walker Brown was born with a genetic mutation so rare that doctors call it an orphan syndrome: perhaps 300 people around the world also live with it. Walker turns twelve in 2008, but he weighs only 54 pounds, is still in diapers, can't speak and needs to wear special cuffs on his arms so th
SUMMARY: Walker Brown was born with a genetic mutation so rare that doctors call it an orphan syndrome: perhaps 300 people around the world also live with it. Walker turns twelve in 2008, but he weighs only 54 pounds, is still in diapers, can't speak and needs to wear special cuffs on his arms so th
SUMMARY: Walker Brown was born with a genetic mutation so rare that doctors call it an orphan syndrome: perhaps 300 people around the world also live with it. Walker turns twelve in 2008, but he weighs only 54 pounds, is still in diapers, can't speak and needs to wear special cuffs on his arms so th