Global Variome shared LOVD

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Phenotype #0000350693 Individual ID 00464560 Associated disease MRXS35 Phenotype details fetal growth delay, microcephaly, microretrognathia, protruding ears, nasal bridge collapse and high-arched palate Diagnosis/Initial - Inheritance Isolated (sporadic) Diagnosis/Definite - Age/Examination - Age/Onset - Phenotype/Onset - Protein - Owner name Ke Wu Database submission license Creative Commons Attribution-NonCommercial 4.0 International Created by Ke Wu Date created 2025-04-14 03:38:46 +02:00 (CEST) Date last edited 2025-04-14 11:23:41 +02:00 (CEST)

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