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| Imprinting disorders v2.1 | Sarah Milton Copied Region ISCA-37447-Loss from panel Intellectual disability syndromic and non-syndromic | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Imprinting disorders v2.1 | ISCA-37447-Loss |
Sarah Milton Region: ISCA-37447-Loss was added Region: ISCA-37447-Loss was added to Imprinting disorders. Sources: ClinGen,Expert Review Green,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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