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Cited by in F6Publishing
For: Lavillaureix A, Foulon G, Launay E, Belaud-Rotureau MA, Thibault R, Lambe C, Aussel D, Pasquier L, Odent S, Arnaud A, Habonimana E, Dabadie A, Jaillard S. Antenatal finding of 16q24.1 duplication including FOXF1, revealing an autosomal dominant familial pathology with congenital short bowel, malrotation and renal abnormalities. Clin Res Hepatol Gastroenterol 2021;45:101562. [PMID: 33208297 DOI: 10.1016/j.clinre.2020.10.007] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
Number Citing Articles
1 Li L, Chu C, Li S, Lu D, Zheng P, Sheng J, Luo LJ, Wu X, Zhang YD, Yin C, Duan AH. Renal agenesis-related genes are associated with Herlyn-Werner-Wunderlich syndrome. Fertil Steril 2021:S0015-0282(21)00533-1. [PMID: 34311961 DOI: 10.1016/j.fertnstert.2021.06.033] [Cited by in Crossref: 2] [Cited by in F6Publishing: 5] [Article Influence: 1.0] [Reference Citation Analysis]