Browse by Author Tullio-Pelet,, A
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| Title | Author(s) | Year | View Count |  | 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, A | 2005 | 97 |
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