TY  - JOUR
AU  - Tang, Clara Sze-Man
AU  - Gui, Hongsheng
AU  - Kapoor, Ashish
AU  - Kim, Jeong-Hyun
AU  - Luzón-Toro, Berta
AU  - Pelet, Anna
AU  - Burzynski, Grzegorz
AU  - Lantieri, Francesca
AU  - So, Man-Ting
AU  - Berrios, Courtney
AU  - Shin, Hyoung Doo
AU  - Fernández, Raquel M
AU  - Le, Thuy-Linh
AU  - Verheij, Joke B G M
AU  - Matera, Ivana
AU  - Cherny, Stacey S
AU  - Nandakumar, Priyanka
AU  - Cheong, Hyun Sub
AU  - Antiñolo, Guillermo
AU  - Amiel, Jeanne
AU  - Seo, Jeong-Meen
AU  - Kim, Dae-Yeon
AU  - Oh, Jung-Tak
AU  - Lyonnet, Stanislas
AU  - Borrego, Salud
AU  - Ceccherini, Isabella
AU  - Hofstra, Robert M W
AU  - Chakravarti, Aravinda
AU  - Kim, Hyun-Young
AU  - Sham, Pak Chung
AU  - Tam, Paul K H
AU  - Garcia-Barceló, Maria-Mercè
PY  - 2016
DO  - 10.1093/hmg/ddw333
UR  - http://hdl.handle.net/10668/10504
T2  - Human molecular genetics
AB  - Hirschsprung disease (HSCR) is the most common cause of neonatal intestinal obstruction. It is characterized by the absence of ganglia in the nerve plexuses of the lower gastrointestinal tract. So far, three common disease-susceptibility variants at...
LA  - en
KW  - Alleles
KW  - Asian People
KW  - Ethnicity
KW  - Female
KW  - Genetic Predisposition to Disease
KW  - Genome-Wide Association Study
KW  - Genotype
KW  - Hirschsprung Disease
KW  - Humans
KW  - Introns
KW  - Male
KW  - Neuregulin-1
KW  - Polymorphism, Single Nucleotide
KW  - Proto-Oncogene Proteins c-ret
KW  - Semaphorin-3A
KW  - White People
TI  - Trans-ethnic meta-analysis of genome-wide association studies for Hirschsprung disease.
TY  - research article
VL  - 25
ER  -