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Cited by in F6Publishing
For: Berland S, Haukanes BI, Juliusson PB, Houge G. Deep exploration of a CDKN1C mutation causing a mixture of Beckwith-Wiedemann and IMAGe syndromes revealed a novel transcript associated with developmental delay. J Med Genet 2020:jmedgenet-2020-107401. [PMID: 33443097 DOI: 10.1136/jmedgenet-2020-107401] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
Number Citing Articles
1 Tolezano GC, Bastos GC, da Costa SS, Freire BL, Homma TK, Honjo RS, Yamamoto GL, Passos-bueno MR, Koiffmann CP, Kim CA, Vianna-morgante AM, de Lima Jorge AA, Bertola DR, Rosenberg C, Krepischi ACV. Burden of Rare Copy Number Variants in Microcephaly: A Brazilian Cohort of 185 Microcephalic Patients and Review of the Literature. J Autism Dev Disord 2022. [DOI: 10.1007/s10803-022-05853-z] [Reference Citation Analysis]
2 Li J, He H, Chen L. CDKN1C gene mutation causing familial Silver–Russell syndrome, with family pedigree.. [DOI: 10.21203/rs.3.rs-2314166/v1] [Reference Citation Analysis]
3 Berland S, Rustad CF, Bentsen MHL, Wollen EJ, Turowski G, Johansson S, Houge G, Haukanes BI. Double paternal uniparental isodisomy 7 and 15 presenting with Beckwith-Wiedemann spectrum features. Cold Spring Harb Mol Case Stud 2021;7:a006113. [PMID: 34615670 DOI: 10.1101/mcs.a006113] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]