SEMA3A rs7804122 polymorphism is associated with Hirschsprung disease in the Northeastern region of China

Semaphorin 3A expression in the colon of Hirschsprung disease

(2011) Li-Li Wang et al.   BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY

A six-generation Chinese family in haplogroup B4C1C exhibits high penetrance of 1555A > G-induced hearing Loss

(2010) Yan Bai et al.   BMC Medical Genetics

Genetic background impacts developmental potential of enteric neural crest-derived progenitors in the Sox10Dom model of Hirschsprung disease

(2010) Lauren C. Walters et al.   HUMAN MOLECULAR GENETICS

Genetic basis of Hirschsprung’s disease

(2009) Paul K. H. Tam et al.   PEDIATRIC SURGERY INTERNATIONAL

Genome-wide association study identifiesNRG1as a susceptibility locus for Hirschsprung's disease

(2009) Maria-Mercè Garcia-Barcelo et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Analysis of East Asia Genetic Substructure Using Genome-Wide SNP Arrays

(2008) Chao Tian et al.   PLoS One