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| BabyScreen+ newborn screening v1.114 | FOXH1 | Tommy Li Added phenotypes Congenital heart defects for gene: FOXH1 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| BabyScreen+ newborn screening v0.0 | FOXH1 |
Zornitza Stark gene: FOXH1 was added gene: FOXH1 was added to gNBS. Sources: Expert Review Red,BabySeq Category C gene Mode of inheritance for gene: FOXH1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Phenotypes for gene: FOXH1 were set to Congenital heart defects |
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