Browsing by Author So, MT

Jump to: 0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
Showing results 41 to 60 of 69 < previous   next >
TitleAuthor(s)Issue DateViews
 
2010
308
 
2016
 
Genetic profile of a multiplex Hirschsprung disease family
Proceeding/Conference:American Society of Human Genetics (ASHG) 2019 Annual Meeting
2019
103
 
Genetic mapping for RET-dependent modifiers in Hirschsprung disease (HSCR)
Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2006
2006
119
 
Gene network analysis of candidate loci for human anorectal malformations
Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2013
2013
71
 
Functional analyses of RET mutations in Chinese hirschsprung disease patients
Journal:Birth Defects Research Part A: Clinical and Molecular Teratology
2012
304
Fine mapping on chromosome 10q24.2 implicates ADD3 in biliary atresia
Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2012
2012
65
Fine mapping of the NRG1 Hirschsprung's-associated gene
Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2010
2010
93
 
2011
183
 
2010
178
 
Fine mapping of Hirschsprung’s disease loci in 9q31
Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2009
2009
 
2005
65
 
Exome sequencing reveals a recessive mechanism involving interacting genes in persistent cloaca
Proceeding/Conference:Annual International Congress of the British Association of Paediatric Surgeons, BAPS 2016
2016
74
 
2006
 
Evaluation of thyroid transcription factor 1 (TTF-1) as a Hirschsprung's disease (HSCR) locus by mutation analysis
Proceeding/Conference:Annual Meeting of the Pacific Association of Pediatric Surgeons, PAPS 2006
2006
160
 
2007
164
 
2018
66
 
Epidemiological and genetic analysis of Banglaeshi Hirschsprung disease patients (Poster presentation)
Proceeding/Conference:The 5th International Symposium on Development of the Enteric Nervous System: cells, signals genes and therapy, 2018
2018
57
 
Deciphering the genetic basis of Hirschsprung disease by whole genome sequencing
Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2016
2016
108
 
2018
32