The association between Hirschsprung's disease and multiple endocrine neoplasia type 2a: A systematic review

Pediatric Surgery International

Volumn 30, Issue 8, 2014, Pages 751-756

  Coyle, David ^a   Friedmacher, Florian ^a   Puri, Prem ^a  

^a OUR LADY S CHILDREN S HOSPITAL   (Ireland)

Author keywords

Hirschsprung's; Janus; MEN2A; MEN2B; Multiple endocrine neoplasia; RET

Indexed keywords

ARTICLE; COLON AGANGLIONOSIS; DISEASE ASSOCIATION; EXON; FAMILY HISTORY; GAIN OF FUNCTION MUTATION; GASTROINTESTINAL SYMPTOM; GENE MUTATION; HIRSCHSPRUNG DISEASE; HUMAN; INCIDENCE; LOSS OF FUNCTION MUTATION; ONCOGENE RET; PHENOTYPE; PREVALENCE; PRIORITY JOURNAL; SIPPLE SYNDROME; SYSTEMATIC REVIEW; CHILD; DNA MUTATIONAL ANALYSIS; GENETICS; METABOLISM; MULTIPLE ENDOCRINE NEOPLASIA TYPE 2A; MUTATION; PEDIGREE;

DNA; PROTEIN RET;

CHILD; DNA MUTATIONAL ANALYSIS; DNA, NEOPLASM; HIRSCHSPRUNG DISEASE; HUMANS; MULTIPLE ENDOCRINE NEOPLASIA TYPE 2A; MUTATION; PEDIGREE; PHENOTYPE; PROTO-ONCOGENE PROTEINS C-RET;

EID: 84908355989     PISSN: 01790358     EISSN: 14379813     Source Type: Journal    
DOI: 10.1007/s00383-014-3538-2     Document Type: Article

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