| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Genetic Epilepsy v1.308 | Sarah Milton Copied Region ISCA-37404-Loss from panel Common deletion and duplication syndromes | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genetic Epilepsy v1.308 | ISCA-37404-Loss |
Sarah Milton Region: ISCA-37404-Loss was added Region: ISCA-37404-Loss was added to Genetic Epilepsy. Sources: Expert Review Green,Expert list SV/CNV tags were added to Region: ISCA-37404-Loss. Mode of inheritance for Region: ISCA-37404-Loss was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Publications for Region: ISCA-37404-Loss were set to 20301323; 20301505 Phenotypes for Region: ISCA-37404-Loss were set to Angelman syndrome, MIM# 105830; Prader-Willi syndrome, MIM# 176270 |
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