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Highly recurrent RET mutations and novel mutations in genes of the receptor tyrosine kinase and endothelin receptor B pathways in Chinese patients with sporadic Hirschsprung disease.
Clin Chem. 2004 Jan;50(1):93-100. doi: 10.1373/clinchem.2003.022061. Epub 2003 Nov 18.
Clin Chem. 2004.
PMID: 14633923
Endothelin-3 gene mutations in isolated and syndromic Hirschsprung disease.
Bidaud C, Salomon R, Van Camp G, Pelet A, Attié T, Eng C, Bonduelle M, Amiel J, Nihoul-Fékété C, Willems PJ, Munnich A, Lyonnet S.
Bidaud C, et al.
Eur J Hum Genet. 1997 Jul-Aug;5(4):247-51.
Eur J Hum Genet. 1997.
PMID: 9359047
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