Global Variome shared LOVD

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Phenotype #0000041467 Individual ID 00054752 Associated disease BWS Phenotype details see paper; ..., placental mesenchymal dysplasia; abdominal wall defect (HP:0010866); Diagnosis/Initial - Inheritance Familial Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Jasmin Beygo Database submission license No license selected Created by Jasmin Beygo Date created 2015-11-24 11:31:20 +01:00 (CET) Date last edited 2020-04-07 10:37:40 +02:00 (CEST)

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