| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Fetal anomalies v2.67 | Sarah Milton Copied Region ISCA-37447-Loss from panel Common deletion and duplication syndromes | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v2.67 | ISCA-37447-Loss |
Sarah Milton Region: ISCA-37447-Loss was added Region: ISCA-37447-Loss was added to Fetal anomalies. Sources: Expert Review Green,ClinGen SV/CNV tags were added to Region: ISCA-37447-Loss. Mode of inheritance for Region: ISCA-37447-Loss was set to MONOALLELIC, autosomal or pseudoautosomal, maternally imprinted (paternal allele expressed) Publications for Region: ISCA-37447-Loss were set to 41926606; 39446997 Phenotypes for Region: ISCA-37447-Loss were set to Temple syndrome MIM#616222; Kagami-Ogata syndrome MIM#608149 |
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