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Skeletal dysplasia, global developmental delay, and multiple congenital anomalies in a 5-year-old boy-Report of the second family with B3GAT3 mutation and expansion of the phenotype

✍ Scribed by von Oettingen, Julia E.; Tan, Wen-Hann; Dauber, Andrew


Book ID
125425407
Publisher
John Wiley and Sons
Year
2014
Tongue
English
Weight
196 KB
Volume
164
Category
Article
ISSN
1552-4825

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