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29 Apr 2019	Fetal anomalies v0.222	TGFBR2	Rebecca Foulger edited their review of gene: TGFBR2: Added comment: This gene and phenotype were reviewed during meetings at Great Ormond Street hospital in March and April 2019. Clinical review and curation was performed by Lyn Chitty, Anna de Burca, Rhiannon Mellis, Richard Scott, Ellen McDonagh and Rebecca Foulger. Outcome of review: Confirmed that phenotype is fetally-relevant: include on the Fetal anomalies panel as a Green gene.; Changed rating: GREEN
11 Dec 2018	Fetal anomalies v0.9	TGFBR2	Rebecca Foulger reviewed gene: TGFBR2: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
08 Nov 2018	Fetal anomalies v0.1	TGFBR2	Rebecca Foulger Added phenotypes TGFBR2-RELATED LOEYS-DIETZ SYNDROME for gene: TGFBR2
08 Nov 2018	Fetal anomalies v0.1	TGFBR2	Rebecca Foulger gene: TGFBR2 was added gene: TGFBR2 was added to Fetal anomalies. Sources: Expert Review Green,PAGE DD-Gene2Phenotype Mode of inheritance for gene: TGFBR2 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Phenotypes for gene: TGFBR2 were set to LOEYS-DIETZ SYNDROME