Increased prevalence of mutations in the cystic fibrosis transmembrane conductance regulator in children with chronic rhinosinusitis.

Pediatrics

Volumn 109, Issue 1, 2002, Pages

  Raman, Vidya ^a   Clary, Randall ^a   Siegrist, Karen L ^a   Zehnbauer, Barbara ^a   Chatila, Talal A ^a  

^a ST LOUIS CHILDREN S HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CFTR PROTEIN, HUMAN; TRANSMEMBRANE CONDUCTANCE REGULATOR;

ADOLESCENT; ARTICLE; CAUCASIAN; CHILD; CHRONIC DISEASE; FEMALE; GENETIC SCREENING; GENETICS; GENOTYPE; GRAM NEGATIVE INFECTION; HUMAN; INFANT; MALE; MUTATION; PRESCHOOL CHILD; PREVALENCE; RECURRENT DISEASE; RHINITIS; SINUSITIS; SWEATING;

ADOLESCENT; CHILD; CHILD, PRESCHOOL; CHRONIC DISEASE; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; EUROPEAN CONTINENTAL ANCESTRY GROUP; FEMALE; GENETIC SCREENING; GENOTYPE; HUMANS; INFANT; MALE; MUTATION; PREVALENCE; PSEUDOMONAS INFECTIONS; RECURRENCE; RHINITIS; SINUSITIS; SWEATING;

MLCS; MLOWN;

EID: 0036357890     PISSN: None     EISSN: 10984275     Source Type: Journal    
DOI: 10.1542/peds.109.1.e13     Document Type: Article

References (0)