In brief: Hirschsprung disease

Pediatrics in Review

Volumn 27, Issue 8, 2006, Pages

  Feldman, Tamara ^a   Wershil, Barry K ^a   Adam, Henry M ^b  

^a CHILDREN S HOSPITAL AT MONTEFIORE   (United States)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

AGANGLIONOSIS; BARDET BIEDL SYNDROME; ENDOCRINE TUMOR; ENTEROCOLITIS; GENETIC ANALYSIS; HIRSCHSPRUNG DISEASE; HUMAN; INCIDENCE; INTESTINE MOTILITY; NOTE; RECTUM BIOPSY; SMITH LEMLI OPITZ SYNDROME; WAARDENBURG SYNDROME; ARTICLE; CHILD; COMPARATIVE STUDY; CONGENITAL MALFORMATION; FEMALE; GENETICS; INFANT; MALE; NEWBORN; SEXUAL DEVELOPMENT;

ABNORMALITIES; CHILD; FEMALE; HIRSCHSPRUNG DISEASE; HUMANS; INFANT; INFANT, NEWBORN; MALE; SEX CHARACTERISTICS;

EID: 33750961611     PISSN: 01919601     EISSN: 15263347     Source Type: Journal    
DOI: 10.1542/pir.27-8-e56     Document Type: Note

References (0)