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Cited by in F6Publishing
For: Brereton RE, Nickerson SL, Woodward KJ, Edwards T, Sivamoorthy S, Ramos Vasques Walters F, Chabros V, Marchin V, Grumball T, Kennedy D, Uzaraga J, Peverall J, Arscott G, Beilby J, Choong CS, Townshend S, Azmanov DN. Further heterogeneity in Silver-Russell syndrome: PLAG1 deletion in association with a complex chromosomal rearrangement. Am J Med Genet A 2021. [PMID: 34223693 DOI: 10.1002/ajmg.a.62391] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
Number Citing Articles
1 Jauss RT, Schließke S, Abou Jamra R. Routine Diagnostics Confirm Novel Neurodevelopmental Disorders. Genes (Basel) 2022;13. [PMID: 36553572 DOI: 10.3390/genes13122305] [Reference Citation Analysis]
2 Baba N, Lengyel A, Pinti E, Yapici E, Schreyer I, Liehr T, Fekete G, Eggermann T. Microdeletions in 1q21 and 8q12.1 depict two additional molecular subgroups of Silver-Russell syndrome like phenotypes. Mol Cytogenet 2022;15:19. [PMID: 35562807 DOI: 10.1186/s13039-022-00596-z] [Reference Citation Analysis]
3 Loid P, Lipsanen-Nyman M, Ala-Mello S, Hannula-Jouppi K, Kere J, Mäkitie O, Muurinen M. Case report: A novel de novo IGF2 missense variant in a Finnish patient with Silver-Russell syndrome. Front Pediatr 2022;10:969881. [PMID: 36268036 DOI: 10.3389/fped.2022.969881] [Reference Citation Analysis]