Browsing by Author Lyonnet, S

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Showing results 1 to 14 of 14
TitleAuthor(s)Issue DateViews
 
2010
329
 
Differential liabilities of coding and non-coding mutations in complex disease
Proceeding/Conference:American Society of Human Genetics Annual Meeting
2005
37
 
Differential liabilities of rare coding and common non-coding RET mutations explain the multifactorial genetics of Hirschsprung disease.
Proceeding/Conference:Gordon Research Conference on Human Genetics and Genomics Salve Regina University Newport, RI, USA, July 24-29, 2005
2005
50
 
Exonic de novo mutations in sporadic Hirschsprung disease
Proceeding/Conference:European Journal of Human Genetics
2014
51
 
1996
40
 
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
36
 
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
52
 
2008
180
 
2009
9
 
The International Hirschsprung's Disease Consortium: differential liabiilties of coding and non-coding mutations in complex disease
Proceeding/Conference:53rd Annual International Congress of the British Association of Paediatric Suregons, Stockholm, Sweden, 18-21 July 2006
2006
54
 
2009
23
 
2012
48
2013
48
 
2014
72