| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Fetal anomalies v1.544 | Sarah Milton Copied gene TOMM7 from panel Mendeliome | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v1.544 | TOMM7 |
Sarah Milton gene: TOMM7 was added gene: TOMM7 was added to Fetal anomalies. Sources: Expert Review Amber,Literature Mode of inheritance for gene: TOMM7 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: TOMM7 were set to 36299998; 36282599 Phenotypes for gene: TOMM7 were set to Garg-Mishra progeroid syndrome, MIM# 620601 |
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