Functional haplotypes of the RET proto-oncogene promoter are associated with Hirschsprung disease (HSCR)

By Fitze Guido  

Human Molecular Genetics, Vol. 12, Iss. 24, 2003-12 ,pp. : 3207-3214

Oxford University Press

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Mutation of the RET ligand, neurturin, supports multigenic inheritance in Hirschsprung disease

By Bachy B.  

Human Molecular Genetics, Vol. 7, Iss. 9, 1998-09 ,pp. : 1449-1452

Oxford University Press

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Intrinsic susceptibility to misfolding of a hot-spot for Hirschsprung disease mutations in the ectodomain of RET

By Kjær Svend   Ibáñez Carlos F.  

Human Molecular Genetics, Vol. 12, Iss. 17, 2003-09 ,pp. : 2133-2144

Oxford University Press

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Reduced RET expression in gut tissue of individuals carrying risk alleles of Hirschsprung's disease

By Miao Xiaoping   Leon Thomas Yuk-Yu   Ngan Elly Sau-Wai   So Man-Ting   Yuan Zheng-Wei   Lui Vincent Chi-Hang   Chen Yan   Wong Kenneth Kak-Yuen   Tam Paul Kwong-Hang   Garcia-Barcel Merc  

Human Molecular Genetics, Vol. 19, Iss. 8, 2010-04 ,pp. : 1461-1467

Oxford University Press

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Hirschsprung disease in MEN 2A: increased spectrum of RET exon 10 genotypes and strong genotype–phenotype correlation

By Decker R.A.  

Human Molecular Genetics, Vol. 7, Iss. 1, 1998-01 ,pp. : 129-134

Oxford University Press

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