Homozygosity for a frequent and weakly penetrant predisposing allele at the RET locus in sporadic Hirschsprung disease

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Bibliographic Details
Main Authors:	Pelet, A, de Pontual, L, Clement-Ziza, M, Salomon, R, Mugnier, C, Matsuda, F, Lathrop, M, Munnich, A, Feingold, J, Lyonnet, S, Abel, L, Amiel, J
Format:	Artigo
Language:	Inglês
Published:	BMJ Group 2005
Subjects:	Electronic Letter
Online Access:	https://ncbi.nlm.nih.gov/pmc/articles/PMC1736014/ https://ncbi.nlm.nih.gov/pubmed/15744028 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2004.028746
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