Genetic counseling and neonatal screening for cystic fibrosis: An assessment of the communication process

Pediatrics

Volumn 107, Issue 4 I, 2001, Pages 699-705

  Ciske, David J ^a   Haavisto, Amy ^a   Laxova, Anita ^a   Rock, Lan Zeng Michael ^a   Farrell, Philip M ^a  

^a UNIVERSITY OF WISCONSIN SCHOOL OF MEDICINE AND PUBLIC HEALTH   (United States)

Author keywords

Cystic fibrosis; Genetic counseling; Heterozygote; Newborn screening; Risk communication

Indexed keywords

ARTICLE; CYSTIC FIBROSIS; FOLLOW UP; GENETIC COUNSELING; HEALTH EDUCATION; HETEROZYGOTE; HUMAN; INFANT; INTERPERSONAL COMMUNICATION; MAJOR CLINICAL STUDY; NEWBORN; NEWBORN SCREENING; PARENT; PARENTAL BEHAVIOR; PRIORITY JOURNAL; QUESTIONNAIRE; SWEAT TEST;

ADULT; ATTITUDE TO HEALTH; CHILD, PRESCHOOL; CHLORIDES; COMMUNICATION; CYSTIC FIBROSIS; ELECTROLYTES; FEMALE; GENETIC COUNSELING; HEALTH KNOWLEDGE, ATTITUDES, PRACTICE; HETEROZYGOTE DETECTION; HUMANS; INFANT; INFANT, NEWBORN; MALE; NEONATAL SCREENING; PARENTS; PROFESSIONAL-FAMILY RELATIONS; QUESTIONNAIRES; RETROSPECTIVE STUDIES; SWEAT; WISCONSIN;

EID: 0035068566     PISSN: 00314005     EISSN: None     Source Type: Journal    
DOI: 10.1542/peds.107.4.699     Document Type: Article

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