| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Microcephaly v1.373 | Sarah Milton Copied Region ISCA-37390-Loss from panel Common deletion and duplication syndromes | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Microcephaly v1.373 | ISCA-37390-Loss |
Sarah Milton Region: ISCA-37390-Loss was added Region: ISCA-37390-Loss was added to Microcephaly. Sources: Expert Review Green,Expert Review SV/CNV tags were added to Region: ISCA-37390-Loss. Mode of inheritance for Region: ISCA-37390-Loss was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for Region: ISCA-37390-Loss were set to 16953888 Phenotypes for Region: ISCA-37390-Loss were set to Cri-du-chat syndrome MIM#123450; intellectual disability; microcephaly |
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