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Hirschsprung disease, associated syndromes and genetics: a review.
Amiel J, Sproat-Emison E, Garcia-Barcelo M, Lantieri F, Burzynski G, Borrego S, Pelet A, Arnold S, Miao X, Griseri P, Brooks AS, Antinolo G, de Pontual L, Clement-Ziza M, Munnich A, Kashuk C, West K, Wong KK, Lyonnet S, Chakravarti A, Tam PK, Ceccherini I, Hofstra RM, Fernandez R; Hirschsprung Disease Consortium. Amiel J, et al. Among authors: wong kk. J Med Genet. 2008 Jan;45(1):1-14. doi: 10.1136/jmg.2007.053959. Epub 2007 Oct 26. J Med Genet. 2008. PMID: 17965226 Review.
Evaluation of the NK2 homeobox 1 gene (NKX2-1) as a Hirschsprung's disease locus.
Garcia-Barceló MM, Lau DK, Ngan ES, Leon TY, Liu T, So M, Miao X, Lui VC, Wong KK, Ganster RW, Cass DT, Croaker GD, Tam PK. Garcia-Barceló MM, et al. Among authors: wong kk. Ann Hum Genet. 2008 Mar;72(Pt 2):170-7. doi: 10.1111/j.1469-1809.2007.00403.x. Epub 2007 Dec 12. Ann Hum Genet. 2008. PMID: 18081917 Retracted.
1,756 results