Browsing by Author Lyonnet, S

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Showing results 1 to 19 of 19
TitleAuthor(s)Issue DateViews
 
2019
127
 
2010
171
 
Differential liabilities of coding and non-coding mutations in complex disease
Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2005
2005
145
 
2005
176
 
Exonic de novo mutations in sporadic Hirschsprung disease
Proceeding/Conference:European Journal of Human Genetics
2014
83
 
2020
9
 
1996
151
 
Heterozygous endothelin receptor B mutation in isolated Hirschsprung's disease
Proceeding/Conference:Annual International Congress of British Association of Paediatric Surgeons
1996
178
 
Higher prevalence of Hirschsprung disease in China explained by a common RET mutation
Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2006
2006
141
 
2008
221
 
2009
87
 
The International Hirschsprung's Disease Consortium: differential liabiilties of coding and non-coding mutations in complex disease
Proceeding/Conference:Annual International Congress of the British Association of Paediatric Suregons, BAPS 2006
2006
134
 
2009
73
 
2012
77
 
2020
37
2013
116
 
2014
69
 
2016
104
 
2017
99