Global Variome shared LOVD

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Phenotype #0000092567 Individual ID 00043792 Associated disease KDVS Phenotype details 17q21.31 deletion syndrome, see paper; … Diagnosis/Initial - Inheritance Isolated (sporadic) Diagnosis/Definite - Age/Examination 5y6m (5 years, 6 months) Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name David Koolen Database submission license No license selected Created by David Koolen Date created 2015-06-20 15:39:31 +02:00 (CEST) Date last edited N/A

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