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| Genomic imprinting v0.26 | FGF12 | Sarah Leigh reviewed gene: FGF12: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genomic imprinting v0.21 | FGF12 |
Sarah Leigh gene: FGF12 was added gene: FGF12 was added to Imprinted Genes. Sources: Literature Mode of inheritance for gene: FGF12 was set to MONOALLELIC, autosomal or pseudoautosomal, maternally imprinted (paternal allele expressed) Publications for gene: FGF12 were set to 27835649; 30794780 |
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