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| BabyScreen+ newborn screening v1.114 | CCDC50 |
Tommy Li Added phenotypes Deafness, autosomal dominant 44 , MIM# 607453 for gene: CCDC50 Publications for gene CCDC50 were updated from 27911912; 24875298; 17503326 to 17503326; 27911912; 24875298 |
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| BabyScreen+ newborn screening v0.0 | CCDC50 |
Zornitza Stark gene: CCDC50 was added gene: CCDC50 was added to gNBS. Sources: Expert Review Red,BabySeq Category C gene Mode of inheritance for gene: CCDC50 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: CCDC50 were set to 27911912; 24875298; 17503326 Phenotypes for gene: CCDC50 were set to Deafness, autosomal dominant 44 , MIM# 607453 |
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