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A novel skeletal dysplasia with developmental delay and acanthosis nigricans is caused by a Lys650Met mutation in the fibroblast growth factor receptor 3 gene.
Tavormina PL, Bellus GA, Webster MK, Bamshad MJ, Fraley AE, McIntosh I, Szabo J, Jiang W, Jabs EW, Wilcox WR, Wasmuth JJ, Donoghue DJ, Thompson LM, Francomano CA. Tavormina PL, et al. Among authors: szabo j. Am J Hum Genet. 1999 Mar;64(3):722-31. doi: 10.1086/302275. Am J Hum Genet. 1999. PMID: 10053006 Free PMC article.
Epileptiform discharges in the anterior thalamus of epilepsy patients.
Jordán Z, Szabó JP, Sákovics A, Kelemen A, Halász L, Erőss L, Fabó D. Jordán Z, et al. Among authors: szabo jp. iScience. 2024 Mar 27;27(5):109582. doi: 10.1016/j.isci.2024.109582. eCollection 2024 May 17. iScience. 2024. PMID: 38726366 Free PMC article.
Acute Myelomonoblastic Leukemia (My1/De): A Preclinical Rat Model.
Arató V, Képes Z, Szabó JP, Farkasinszky G, Sass T, Dénes N, Kis A, Opposits G, Jószai I, Kálmán FK, Hajdu I, Trencsényi G, Kertész I. Arató V, et al. Among authors: szabo jp. In Vivo. 2024 May-Jun;38(3):1064-1073. doi: 10.21873/invivo.13540. In Vivo. 2024. PMID: 38688644 Free PMC article.
771 results