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| Genomic newborn screening: BabyScreen+ v0.0 | NKX3-2 | Zornitza Stark gene: NKX3-2 was added gene: NKX3-2 was added to gNBS. Sources: Expert Review Red,BabySeq Category C gene Mode of inheritance for gene: NKX3-2 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: NKX3-2 were set to Spondylo-megaepiphyseal-metaphyseal dysplasia | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||