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| BabyScreen+ newborn screening v1.114 | VWF | Tommy Li Added phenotypes von Willebrand disease for gene: VWF | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| BabyScreen+ newborn screening v0.0 | VWF |
Zornitza Stark gene: VWF was added gene: VWF was added to gNBS. Sources: Expert Review Amber,BabySeq Category B gene Mode of inheritance for gene: VWF was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Phenotypes for gene: VWF were set to von Willebrand disease |
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