Report of two patients with associated conditions in addition to cystic fibrosis

Journal of Cystic Fibrosis

Volumn 9, Issue 4, 2010, Pages 269-271

  Jambhekar, Supriya K ^a   Carroll, John L ^a   Keiles, Steven ^b  

^a UNIVERSITY OF ARKANSAS FOR MEDICAL SCIENCES   (United States)

^b AMBRY GENETICS   (United States)

Author keywords

Associated conditions; Crohn's disease; Cystic fibrosis; Cystic fibrosis transmembrane conductance regulator; Gene sequence analysis; Genetics; Mutation; Rubinstein Taybi syndrome

Indexed keywords

ANTIBIOTIC AGENT; DNA; DORNASE ALFA; INFLIXIMAB; INSULIN; PANCREAS ENZYME; TRANSMEMBRANE CONDUCTANCE REGULATOR; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR;

ARTICLE; CASE REPORT; CHILD; CLINICAL FEATURE; COMPRESSION THERAPY; CROHN DISEASE; CYSTIC FIBROSIS; DIABETES MELLITUS; DNA DETERMINATION; FAILURE TO THRIVE; FEMALE; GASTROINTESTINAL SYMPTOM; GEL ELECTROPHORESIS; GENE MUTATION; GENETIC ASSOCIATION; GROWTH DISORDER; HUMAN; LACTOSE INTOLERANCE; LUNG FUNCTION TEST; MALE; MULTIPLEX LIGATION DEPENDENT PROBE AMPLIFICATION; MUTATIONAL ANALYSIS; PANCREAS INSUFFICIENCY; RESPIRATORY TRACT INFECTION; RUBINSTEIN SYNDROME; SCHOOL CHILD; SEQUENCE ANALYSIS; THORAX RADIOGRAPHY; AFRICAN AMERICAN; CAUCASIAN; COMPLICATION; GENE DELETION; GENETICS; MUTATION; SINGLE NUCLEOTIDE POLYMORPHISM;

AFRICAN AMERICANS; CHILD; CROHN DISEASE; CYSTIC FIBROSIS; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; EUROPEAN CONTINENTAL ANCESTRY GROUP; FEMALE; GENE DELETION; HUMANS; MALE; MUTATION; POLYMORPHISM, SINGLE NUCLEOTIDE; RUBINSTEIN-TAYBI SYNDROME;

EID: 77953915632     PISSN: 15691993     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jcf.2010.04.007     Document Type: Article

References (7)

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