Detalhe da pesquisa
1.
Genome-wide association study and mouse model identify interaction between RET and EDNRB pathways in Hirschsprung disease.
Nat Genet
; 32(2): 237-44, 2002 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-12355085
2.
A common sex-dependent mutation in a RET enhancer underlies Hirschsprung disease risk.
Nature
; 434(7035): 857-63, 2005 Apr 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-15829955
3.
Population bottlenecks as a potential major shaping force of human genome architecture.
PLoS Genet
; 3(7): e119, 2007 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-17658953
4.
Phenotype-genotype correlation in Hirschsprung disease is illuminated by comparative analysis of the RET protein sequence.
Proc Natl Acad Sci U S A
; 102(25): 8949-54, 2005 Jun 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-15956201