Global Variome shared LOVD

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Phenotype #0000309911 Individual ID 00418574 Associated disease SGS Phenotype details see paper (extensive phenotyping) Diagnosis/Initial Shprintzen-Goldberg craniosynostosis syndrome Inheritance Familial, autosomal dominant Diagnosis/Definite SGS Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2022-09-30 10:17:41 +02:00 (CEST) Date last edited N/A

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