TY  - GEN
AU  - Nagaya,Masahiro
AU  - Kato,Junji
AU  - Niimi,Norihiro
AU  - Tanaka,Shuiti
AU  - Wakamatsu,Nobuaki
TI  - Clinical features of a form of Hirschsprung's disease caused by a novel genetic abnormality
SN  - 1531-5037
PY  - 2002///0905
KW  - Adult
KW  - Child
KW  - Chromosome Mapping
KW  - Chromosomes, Human, Pair 13
KW  - Chromosomes, Human, Pair 2
KW  - Codon, Nonsense
KW  - DNA-Binding Proteins
KW  - metabolism
KW  - Female
KW  - Hirschsprung Disease
KW  - diagnosis
KW  - Homeodomain Proteins
KW  - genetics
KW  - Humans
KW  - Infant, Newborn
KW  - Male
KW  - Repressor Proteins
KW  - Retrospective Studies
KW  - Sequence Deletion
KW  - Smad Proteins
KW  - Trans-Activators
KW  - Translocation, Genetic
KW  - Zinc Finger E-box Binding Homeobox 2
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1053/jpsu.2002.34455
ER  -