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De novo exon 1 missense mutations of SKI and Shprintzen-Goldberg syndrome: Two new cases and a clinical review

✍ Scribed by Au, P.Y. Billie; Racher, Hilary E.; Graham, John M.; Kramer, Nancy; Lowry, R. Brian; Parboosingh, Jillian S.; Innes, A. Micheil


Book ID
125418345
Publisher
John Wiley and Sons
Year
2013
Tongue
English
Weight
627 KB
Volume
164
Category
Article
ISSN
1552-4825

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