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COMP mutation screening as an aid for the clinical diagnosis and counselling of patients with a suspected diagnosis of pseudoachondroplasia or multiple epiphyseal dysplasia

✍ Scribed by Kennedy, Jason; Jackson, Gail; Ramsden, Simon; Taylor, Jacky; Newman, William; Wright, Michael J; Donnai, Dian; Elles, Rob; Briggs, Michael D


Book ID
110026178
Publisher
Nature Publishing Group
Year
2005
Tongue
English
Weight
109 KB
Volume
13
Category
Article
ISSN
1018-4813

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