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Query Trace: Down Syndrome and RET[original query]

Interaction between a chromosome 10 RET enhancer and chromosome 21 in the Down syndrome-Hirschsprung disease association. Human mutation 2009 Mar . Arnold S, Pelet A, Amiel J, Borrego S, Hofstra R, Tam P, Ceccherini I, Lyonnet S, Sherman S, Chakravarti A Similar articles in PubMed
Epistatic interactions with a common hypomorphic RET allele in syndromic Hirschsprung disease. Human mutation 2007 Aug 28 (8): 790-6. de Pontual L, Pelet A, Clement-Ziza M, Trochet D, Antonarakis S E, Attie-Bitach T, Beales P L, Blouin J-L, Dastot-Le Moal F, Dollfus H, Goossens M, Katsanis N, Touraine R, Feingold J, Munnich A, Lyonnet S, Amiel Similar articles in PubMed