Clinical features of a form of Hirschsprung's disease caused by a novel genetic abnormality

Journal of Pediatric Surgery

Volumn 37, Issue 8, 2002, Pages 1117-1122

  Nagaya, Masahiro ^a,b,c   Kato, Junji ^a,b,c   Niimi, Norihiro ^a,b,c   Tanaka, Shuiti ^a,b,c   Wakamatsu, Nobuaki ^a,b,c  

^a Central Hospital   (Japan)

^b INSTITUTE FOR DEVELOPMENTAL RESEARCH   (Japan)

^c Aichi Prefectural Colony (Human Service Center)   (Japan)

Author keywords

Hirschsprung's disease; Neural crest; ZFHX1B

Indexed keywords

COMPLEMENTARY DNA; GENE PRODUCT; SMAD INTERACTING PROTEIN 1; SMAD PROTEIN; UNCLASSIFIED DRUG;

ARTICLE; CASE REPORT; CLINICAL FEATURE; CORRELATION ANALYSIS; EMBRYO DEVELOPMENT; EPILEPSY; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE FUNCTION; GENE LOCATION; GENE MUTATION; HIRSCHSPRUNG DISEASE; HUMAN; KARYOTYPE; MALE; MENTAL DEFICIENCY; MICROCEPHALY; MULTIGENE FAMILY; NEURAL CREST; PATHOGENESIS; PHYSICAL DISABILITY; PRIORITY JOURNAL; RETROSPECTIVE STUDY; STRABISMUS;

EID: 0036325992     PISSN: 00223468     EISSN: None     Source Type: Journal    
DOI: 10.1053/jpsu.2002.34455     Document Type: Article

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