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BabyScreen+ newborn screening v1.114 | ARL13B | Tommy Li Added phenotypes Joubert syndrome for gene: ARL13B | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
BabyScreen+ newborn screening v0.0 | ARL13B |
Zornitza Stark gene: ARL13B was added gene: ARL13B was added to gNBS. Sources: Expert Review Red,BabySeq Category C gene Mode of inheritance for gene: ARL13B was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: ARL13B were set to Joubert syndrome |