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For: Alhendi ASN, Lim D, McKee S, McEntagart M, Tatton-Brown K, Temple IK, Davies JH, Mackay DJG. Whole-genome analysis as a diagnostic tool for patients referred for diagnosis of Silver-Russell syndrome: a real-world study. J Med Genet 2021:jmedgenet-2021-107699. [PMID: 34135092 DOI: 10.1136/jmedgenet-2021-107699] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 2.0] [Reference Citation Analysis]
Number Citing Articles
1 van der Kaay DCM, Rochtus A, Binder G, Kurth I, Prawitt D, Netchine I, Johannsson G, Hokken-Koelega ACS, Elbracht M, Eggermann T. Comprehensive genetic testing approaches as the basis for personalized management of growth disturbances: current status and perspectives. Endocr Connect 2022;11:e220277. [PMID: 36064195 DOI: 10.1530/EC-22-0277] [Reference Citation Analysis]
2 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. [DOI: 10.3389/fped.2022.969881] [Reference Citation Analysis]
3 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]
4 Mackay DJG, Temple IK. Ongoing Challenges in the Diagnosis of 11p15.5-Associated Imprinting Disorders. Mol Diagn Ther 2022;26:263-72. [PMID: 35522427 DOI: 10.1007/s40291-022-00587-1] [Reference Citation Analysis]