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Prenatal ultrasonographic and molecular diagnosis of Apert syndrome.
Filkins K, Russo JF, Boehmer S, Camous M, Przylepa KA, Jiang W, Jabs EW. Filkins K, et al. Among authors: jiang w. Prenat Diagn. 1997 Nov;17(11):1081-4. doi: 10.1002/(sici)1097-0223(199711)17:11<1081::aid-pd198>3.0.co;2-2. Prenat Diagn. 1997. PMID: 9399359
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: jiang w. Am J Hum Genet. 1999 Mar;64(3):722-31. doi: 10.1086/302275. Am J Hum Genet. 1999. PMID: 10053006 Free PMC article.
Low back pain in China: Disease burden and bibliometric analysis.
Yang WL, Jiang WC, Peng YH, Zhang XJ, Zhou R. Yang WL, et al. Among authors: jiang wc. World J Orthop. 2024 Dec 18;15(12):1200-1207. doi: 10.5312/wjo.v15.i12.1200. eCollection 2024 Dec 18. World J Orthop. 2024. PMID: 39744725 Free PMC article.
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