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panel","entity_name":null,"entity_type":null},{"created":"2022-01-13T18:37:07.618133+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2085","user_name":"Zornitza Stark","item_type":"panel","text":"removed gene:MLH1 from the panel","entity_name":null,"entity_type":null},{"created":"2022-01-13T18:36:39.968065+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2084","user_name":"Zornitza Stark","item_type":"panel","text":"removed gene:MC2R from the panel","entity_name":null,"entity_type":null},{"created":"2022-01-13T18:35:49.686462+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2083","user_name":"Zornitza Stark","item_type":"panel","text":"removed gene:LAMC2 from the panel","entity_name":null,"entity_type":null},{"created":"2022-01-13T18:35:13.061600+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2082","user_name":"Zornitza Stark","item_type":"panel","text":"removed gene:KCNB1 from the panel","entity_name":null,"entity_type":null},{"created":"2022-01-13T18:34:46.597180+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2081","user_name":"Zornitza Stark","item_type":"panel","text":"removed gene:KCNA2 from the panel","entity_name":null,"entity_type":null},{"created":"2022-01-13T18:33:55.868084+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2080","user_name":"Zornitza Stark","item_type":"panel","text":"removed gene:IVD from the panel","entity_name":null,"entity_type":null},{"created":"2022-01-13T18:32:53.336925+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2079","user_name":"Zornitza Stark","item_type":"panel","text":"removed gene:HSD3B7 from the panel","entity_name":null,"entity_type":null},{"created":"2022-01-13T18:31:49.108167+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2078","user_name":"Zornitza Stark","item_type":"panel","text":"removed gene:HMGCS2 from the panel","entity_name":null,"entity_type":null},{"created":"2022-01-13T18:31:22.947672+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2077","user_name":"Zornitza Stark","item_type":"panel","text":"removed gene:HMGCL from the panel","entity_name":null,"entity_type":null},{"created":"2022-01-13T18:31:00.490996+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2076","user_name":"Zornitza Stark","item_type":"panel","text":"removed gene:HEXB from the panel","entity_name":null,"entity_type":null},{"created":"2022-01-13T18:30:26.696868+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2075","user_name":"Zornitza Stark","item_type":"panel","text":"removed gene:HEXA from the panel","entity_name":null,"entity_type":null},{"created":"2022-01-13T18:30:02.823462+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2074","user_name":"Zornitza Stark","item_type":"panel","text":"removed gene:HCN1 from the panel","entity_name":null,"entity_type":null},{"created":"2022-01-13T18:21:38.228223+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2073","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PDE4D as ready","entity_name":"PDE4D","entity_type":"gene"}]}