Associated Papers
Prenatal diagnosis of Silver-Russell syndrome with 8q12 deletion including the PLAG1 gene: a case report and review.
Wu K et al.
Frontiers in Genetics, 2024
Clinical characterization of PLAG1- related Silver-Russell syndrome：A clinical report.
Dong P et al.
European Journal of Medical Genetics, 2023
Further heterogeneity in Silver-Russell syndrome: PLAG1 deletion in association with a complex chromosomal rearrangement.
Brereton RE et al.
American Journal of Medical Genetics. Part A, 2021
Novel Variant in PLAG1 in a Familial Case with Silver-Russell Syndrome Suspicion.
Vado Y et al.
Genes, 2020
33291420 (PubMed )
Supplement: genes-11-01461-s001.zip › genes-1005660 › SUPPLEMENTAL_PLAG1_v2.xlsx › Supplementary_table_s1
Contribution of gene mutations to Silver-Russell syndrome phenotype: multigene sequencing analysis in 92 etiology-unknown patients.
Inoue T et al.
Clinical Epigenetics, 2020
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