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| BabyScreen+ newborn screening v1.114 | B9D2 | Tommy Li Added phenotypes Meckel syndrome for gene: B9D2 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| BabyScreen+ newborn screening v0.0 | B9D2 |
Zornitza Stark gene: B9D2 was added gene: B9D2 was added to gNBS. Sources: Expert Review Red,BabySeq Category C gene Mode of inheritance for gene: B9D2 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: B9D2 were set to Meckel syndrome |
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