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| BabyScreen+ newborn screening v1.114 | MIR96 | Tommy Li Added phenotypes Hearing loss for gene: MIR96 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| BabyScreen+ newborn screening v0.0 | MIR96 |
Zornitza Stark gene: MIR96 was added gene: MIR96 was added to gNBS. Sources: Expert Review Red,BabySeq Category C gene Mode of inheritance for gene: MIR96 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Phenotypes for gene: MIR96 were set to Hearing loss |
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