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For:	Kiraz A, Tubaş F, Seber T. A truncating variant in the THOC6 gene with new findings in a patient with Beaulieu‐Boycott‐Innes syndrome. American J of Med Genetics Pt A. [DOI: 10.1002/ajmg.a.62667] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]

Number	Citing Articles
1	Werren E, Laforce GR, Srivastava A, Perillo DR, Johnson K, Baris S, Berger B, Regan SL, Pfennig CD, de Munnik S, Pfundt R, Hebbar M, Jimenez-heredia R, Karakoc-aydiner E, Ozen A, Dmytrus J, Krolo A, Corning K, Prijoles E, Louie RJ, Lebel RR, Le T, Gordon C, Boztug K, Girish KM, Shukla A, Bielas SL, Schaffer AE. Mechanisms of mRNA processing defects in inherited THOC6 intellectual disability syndrome.. [DOI: 10.1101/2022.09.06.506502] [Reference Citation Analysis]

Number

Citing Articles

Werren E, Laforce GR, Srivastava A, Perillo DR, Johnson K, Baris S, Berger B, Regan SL, Pfennig CD, de Munnik S, Pfundt R, Hebbar M, Jimenez-heredia R, Karakoc-aydiner E, Ozen A, Dmytrus J, Krolo A, Corning K, Prijoles E, Louie RJ, Lebel RR, Le T, Gordon C, Boztug K, Girish KM, Shukla A, Bielas SL, Schaffer AE. Mechanisms of mRNA processing defects in inherited THOC6 intellectual disability syndrome.. [DOI: 10.1101/2022.09.06.506502] [Reference Citation Analysis]