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TypeTitleAuthor(s)YearViews
The International Hirschsprung's Disease Consortium: differential liabiilties of coding and non-coding mutations in complex diseaseTam, PKH; Garcia-Barcelo, MM; Tullio-Pelet, A; Lyonnet, S; Lantieri, F; Kashuk, C; Hofstra, R; Griseri, P; Fernandez, R; Eng, C; Emison, E; Burzynski, G; Ceccherini, I; Borrego, S; Antinolo, G; Amiel, J; West, K; Chakravarti, A2006127
 
Higher prevalence of Hirschsprung disease in China explained by a common RET mutationGarcia-Barcelo, MM; Amiel, J; Antinolo, G; Borrego, S; Burzynski, G; Ceccherini, I; Emison, E; Eng, C; Fernandez, R; Griseri, P; Hofstra, R; Kashuk, C; Lantien, F; Lyonnet, S; Miao, X; Tam, PKH; Tullio-Pelet, A; West, K; Chakravarti, A2006107
 
Differential liabilities of coding and non-coding mutations in complex diseaseBurzynski, G.; Amiel, J.; Antinolo, G; Borrego,, S.; Ceccherini, I; Emison, E; Eng, C; Fernandez, R; Garcia-Barcelo, MM; Griseri, P.; Hofstra, R; Kashuk, C; Lantieri, F; Lyonnet, S; Tam, PKH; Tullio-Pelet, A; West, K; Chakravarti, A200590
 
Differential liabilities of rare coding and common non-coding RET mutations explain the multifactorial genetics of Hirschsprung disease.Emison, E; Burzynski, G; Amiel, J; Borrego, S; Ceccherini,, I; Fernandez, R; Garcia-Barcelo, MM; Griseri, P; Hofstra, R; Kashuk, CS; Lantieri, F; Lyonnet, S; Tam, PKH; Pecina, A; Tullio-Pelet,, A; West, K; Chakravarti, A2005104
 
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