Results 1 to 9 of 9
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TypeTitleAuthor(s)YearViews
Differential contributions of rare and common, coding and noncoding ret mutations to multifactorial hirschsprung disease liabilityEmison, ES; GarciaBarcelo, M; Grice, EA; Lantieri, F; Amiel, J; Burzynski, G; Fernandez, RM; Hao, L; Kashuk, C; West, K; Miao, X; Tam, PKH; Griseri, P; Ceccherini, I; Pelet, A; Jannot, AS; De Pontual, L; HenrionCaude, A; Lyonnet, S; Verheij, JBGM; Hofstra, RMW; Antiñolo, G; Borrego, S; McCallion, AS; Chakravarti, A2010603
 
Dynamic visualization of music classification systemsWest, K; Downie, JS; Hu, X; Jones, MC200845
 
Dynamic classification explorer for music digital librariesDownie, JS; West, K; Hu, X200845
 
Hirschsprung disease, associated syndromes and genetics: A reviewAmiel, J; SproatEmison, E; GarciaBarcelo, M; Lantieri, F; Burzynski, G; Borrego, S; Pelet, A; Arnold, S; Miao, X; Griseri, P; Brooks, AS; Antinolo, G; De Pontual, L; ClementZiza, M; Munnich, A; Kashuk, C; West, K; Wong, KKY; Lyonnet, S; Chakravarti, A; Tam, PKH; Ceccherini, I; Hofstra, RMW; Fernandez, R2008401
 
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, A2005105
 
Chromosomal localization in mouse and human of the vasoactive intestinal peptide receptor type 2 gene: A possible contributor to the holoprosencephaly 3 phenotypeMackay, M; Fantes, J; Scherer, S; Boyle, S; West, K; Tsui, LC; Belloni, E; Lutz, E; Van Heyningen, V; Harmar, AJ1996310
 
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