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A novel genetic syndrome characterized by pediatric cataract, dysmorphism, ectodermal features, and developmental delay in an indigenous Australian family

✍ Scribed by Kathryn P. Burdon; Shane R. Durkin; Mary Burke; Matthew Edwards; John Pater; Tania Straga; Jozef Gecz; Jan E. Liebelt; Jamie E. Craig


Publisher
John Wiley and Sons
Year
2009
Tongue
English
Weight
373 KB
Volume
149A
Category
Article
ISSN
1552-4825

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