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Cited by in F6Publishing
For: Kumps C, D'haenens E, Vergult S, Leus J, van Coster R, Jansen A, Devriendt K, Oostra A, Vanakker OM. Phenotypic spectrum of the RBM10-mediated intellectual disability and congenital malformation syndrome beyond classic TARP syndrome features. Clin Genet 2021;99:449-56. [PMID: 33340101 DOI: 10.1111/cge.13901] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
Number Citing Articles
1 Poulton C, Baynam G, Pugh K, Mason M, Kiraly-Borri C, Gration D, Dreyer L, Viti L, Agostino M, Heng JI. Further evidence for distinct traits associated with RBM10 missense variants. Clin Genet 2022. [PMID: 35645043 DOI: 10.1111/cge.14163] [Reference Citation Analysis]
2 Forman TE, Dennison BJC, Fantauzzo KA. The Role of RNA-Binding Proteins in Vertebrate Neural Crest and Craniofacial Development. J Dev Biol 2021;9:34. [PMID: 34564083 DOI: 10.3390/jdb9030034] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 5.0] [Reference Citation Analysis]