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A novel autosomal recessive malformation syndrome associated with developmental delay and distinctive facies maps to 16ptel in the Hutterite population

✍ Scribed by Kym M. Boycott; Chandree Beaulieu; Erik G. Puffenberger; D. Ross McLeod; Jillian S. Parboosingh; A. Micheil Innes


Publisher
John Wiley and Sons
Year
2010
Tongue
English
Weight
308 KB
Volume
152A
Category
Article
ISSN
1552-4825

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