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Whole exome sequencing coupled with unbiased functional analysis reveals new Hirschsprung disease genes.
Gui H, Schriemer D, Cheng WW, Chauhan RK, Antiňolo G, Berrios C, Bleda M, Brooks AS, Brouwer RW, Burns AJ, Cherny SS, Dopazo J, Eggen BJ, Griseri P, Jalloh B, Le TL, Lui VC, Luzón-Toro B, Matera I, Ngan ES, Pelet A, Ruiz-Ferrer M, Sham PC, Shepherd IT, So MT, Sribudiani Y, Tang CS, van den Hout MC, van der Linde HC, van Ham TJ, van IJcken WF, Verheij JB, Amiel J, Borrego S, Ceccherini I, Chakravarti A, Lyonnet S, Tam PK, Garcia-Barceló MM, Hofstra RM. Gui H, et al. Among authors: lui vc. Genome Biol. 2017 Mar 8;18(1):48. doi: 10.1186/s13059-017-1174-6. Genome Biol. 2017. PMID: 28274275 Free PMC article.
Is there a role for the IHH gene in Hirschsprung's disease?
Garcia-Barceló MM, Lee WS, Sham MH, Lui VC, Tam PK. Garcia-Barceló MM, et al. Among authors: lui vc. Neurogastroenterol Motil. 2003 Dec;15(6):663-8. doi: 10.1046/j.1350-1925.2003.00447.x. Neurogastroenterol Motil. 2003. PMID: 14651602
Esophageal atresia and achalasialike esophageal dysmotility.
Cheng W, Poon KH, Lui VC, Yong JL, Law S, So KT, Tse K, Tam PK. Cheng W, et al. Among authors: lui vc. J Pediatr Surg. 2004 Oct;39(10):1581-3. doi: 10.1016/j.jpedsurg.2004.06.027. J Pediatr Surg. 2004. PMID: 15486912
116 results