Browsing by Author Lyonnet, S

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Showing results 1 to 20 of 20
TitleAuthor(s)Issue DateViews
 
2019
136
 
2010
150
 
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
132
 
2005
161
 
Exonic de novo mutations in sporadic Hirschsprung disease
Proceeding/Conference:European Journal of Human Genetics
2014
59
 
2020
21
 
1996
121
 
Heterozygous endothelin receptor B mutation in isolated Hirschsprung's disease
Proceeding/Conference:Annual International Congress of British Association of Paediatric Surgeons
1996
161
 
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
136
 
2008
207
 
2009
65
 
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
116
 
2009
69
 
2012
58
 
2020
47
2013
148
 
Editor(s):Barsh, GS
2021
9
 
2014
51
 
2016
116
 
2017
107