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| Hand and foot malformations v0.30 | IFT57 | Bryony Thompson Marked gene: IFT57 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Hand and foot malformations v0.30 | IFT57 | Bryony Thompson Gene: ift57 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Hand and foot malformations v0.30 | IFT57 | Bryony Thompson Publications for gene: IFT57 were set to | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Hand and foot malformations v0.0 | IFT57 |
Bryony Thompson gene: IFT57 was added gene: IFT57 was added to Hand and foot malformation. Sources: Expert list Mode of inheritance for gene: IFT57 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: IFT57 were set to ?Orofaciodigital syndrome XVIII MIM#617927 |
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