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Cited by in F6Publishing
For: Prasad M, Balci TB, Prasad C, Andrews JD, Lee R, Jurkiewicz MT, Napier MP, Colaiacovo S, Guillen Sacoto MJ, Karp N. BCL11B-related disorder in two canadian children: Expanding the clinical phenotype. Eur J Med Genet 2020;63:104007. [PMID: 32659295 DOI: 10.1016/j.ejmg.2020.104007] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
Number Citing Articles
1 Santos-Terra J, Deckmann I, Fontes-Dutra M, Schwingel GB, Bambini-Junior V, Gottfried C. Transcription factors in neurodevelopmental and associated psychiatric disorders: A potential convergence for genetic and environmental risk factors. Int J Dev Neurosci 2021. [PMID: 34240460 DOI: 10.1002/jdn.10141] [Reference Citation Analysis]
2 Daher MT, Bausero P, Agbulut O, Li Z, Parlakian A. Bcl11b/Ctip2 in Skin, Tooth, and Craniofacial System. Front Cell Dev Biol 2020;8:581674. [PMID: 33363142 DOI: 10.3389/fcell.2020.581674] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
3 Alfei E, Cattaneo E, Spaccini L, Iascone M, Veggiotti P, Doneda C. Progressive Clinical and Neuroradiological Findings in a Child with BCL11B Missense Mutation: Expanding the Phenotypic Spectrum of Related Disorder. Neuropediatrics 2021. [PMID: 34844266 DOI: 10.1055/s-0041-1736193] [Reference Citation Analysis]