Browsing by Author Lyonnet, S

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Showing results 1 to 14 of 14
TitleAuthor(s)Issue DateViews
 
2010
330
 
Differential liabilities of coding and non-coding mutations in complex disease
Proceeding/Conference:American Society of Human Genetics Annual Meeting
2005
39
 
2005
54
 
Exonic de novo mutations in sporadic Hirschsprung disease
Proceeding/Conference:European Journal of Human Genetics
2014
56
 
1996
42
 
Heterozygous endothelin receptor B mutation in isolated Hirschsprung's disease
Proceeding/Conference:XLIII Annual International Congress of British Association of Paediatric Surgeons, Jersey, UK, July 1996
1996
38
 
Higher prevalence of Hirschsprung disease in China explained by a common RET mutation
Proceeding/Conference:56th Annual Meeting of the American Society of Human Genetics, New Orleans, U.S.A., 9-13 October 2006
2006
55
 
2008
183
 
2009
10
 
The International Hirschsprung's Disease Consortium: differential liabiilties of coding and non-coding mutations in complex disease
Proceeding/Conference:The Annual International Congress of the British Association of Paediatric Suregons
2006
55
 
2009
23
 
2012
51
2013
50
 
2014
72