Associated syndromes Hirschsprung's disease

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^ mäkitie o, heikkinen m, kaitila i, rintala r (2002). hirschsprung s disease in cartilage-hair hypoplasia has poor prognosis . j pediatr surg. 37 (11): 1585–8. doi:10.1053/jpsu.2002.36189. pmid 12407544. 
^ de pontual l, pelet a, clement-ziza m, trochet d, antonarakis se, attie-bitach t, beales pl, blouin jl, dastot-le moal f, dollfus h, goossens m, katsanis n, touraine r, feingold j, munnich a, lyonnet s, amiel j (2007). epistatic interactions common hypomorphic ret allele in syndromic hirschsprung disease . human mutation. 28 (8): 790–6. doi:10.1002/humu.20517. pmid 17397038. 
^ saunders cj, zhao w, ardinger hh (2009). comprehensive zeb2 gene analysis mowat-wilson syndrome in north american cohort: suggested approach molecular diagnostics . american journal of medical genetics. 149a (11): 2527–31. doi:10.1002/ajmg.a.33067. pmid 19842203. 
^ bonnard a, zeidan s, degas v, viala j, baumann c, berrebi d, perrusson o, el ghoneimi (2009). outcomes of hirschsprung s disease associated mowat-wilson syndrome . journal of pediatric surgery. 44 (3): 587–91. doi:10.1016/j.jpedsurg.2008.10.066. pmid 19302864. 
^ mueller c, patel s, irons m, antshel k, salen g, tint gs, bay c (2003). normal cognition , behavior in smith-lemli-opitz syndrome patient presented hirschsprung disease . american journal of medical genetics. 123a (1): 100–6. doi:10.1002/ajmg.a.20491. pmc 1201564 . pmid 14556255. 
^ flori e, girodon e, samama b, becmeur f, viville b, girard-lemaire f, doray b, schluth c, marcellin l, boehm n, goossens m, pingault v (2005). trisomy 7 mosaicism, maternal uniparental heterodisomy 7 , hirschsprung s disease in child silver-russell syndrome . european journal of human genetics. 13 (9): 1013–8. doi:10.1038/sj.ejhg.5201442. pmid 15915162. 






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