Genetic basis of Hirschsprung's disease

Pediatric Surgery International

Volumn 25, Issue 7, 2009, Pages 543-558

  Tam, Paul K H ^a   Garcia Barceló, Mercè ^b  

^a UNIVERSITY OF HONG KONG   (Hong Kong)

^b UNIVERSITY OF HONG KONG   (Hong Kong)

Author keywords

Genetics; Hirschsprungs; RET

Indexed keywords

ENDOTHELIN 3; ENDOTHELIN B RECEPTOR; NEURITE PROMOTING FACTOR; PAIRED MESODERM HOMEOBOX 2B; PROTEIN RET; TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR HOXB5; TRANSCRIPTION FACTOR NKX2.1; TRANSCRIPTION FACTOR SOX10; TRANSCRIPTION FACTOR ZFHX1B; UNCLASSIFIED DRUG;

DISEASE TRANSMISSION; GENE; GENE FREQUENCY; GENE INTERACTION; GENE LOCUS; GENE MUTATION; GENETIC COUNSELING; GENETIC LINKAGE; GENETIC SUSCEPTIBILITY; HIRSCHSPRUNG DISEASE; HUMAN; KIAA1279 GENE; NERVE CELL; NEUROFIBROMATOSIS; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; PROTEIN EXPRESSION; REVIEW; SIGNAL TRANSDUCTION; SIPPLE SYNDROME; SURGICAL TECHNIQUE; SURVIVAL RATE; THYROID MEDULLARY CARCINOMA;

GENETIC PREDISPOSITION TO DISEASE; HIRSCHSPRUNG DISEASE; HUMANS;

EID: 67650710799     PISSN: 01790358     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00383-009-2402-2     Document Type: Review

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