Global Variome shared LOVD

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Phenotype #0000242509 Individual ID 00321298 Associated disease OI Phenotype details Osteogenesis imperfecta Type 2, subtype A, Diagnosis/Initial - Inheritance - Diagnosis/Definite - Age/Examination - Age/Onset - Phenotype/Onset - Protein - Owner name Raymond Dalgleish Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Raymond Dalgleish Date created 2009-07-30 08:44:59 +02:00 (CEST) Date last edited 2013-05-08 14:08:48 +02:00 (CEST)

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