Parental Attitudes toward Genetic Testing for Pediatric Deafness

This publication has 13 references indexed in Scilit:

• Clinical Studies of Families With Hearing Loss Attributable to Mutations in the Connexin 26 Gene (GJB2/DFNB1)
  Pediatrics, 1999
• Attitudes of Deaf Adults toward Genetic Testing for Hereditary Deafness
  American Journal of Human Genetics, 1998
• Connexin26 mutations associated with the most common form of non- syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans
  Human Molecular Genetics, 1997
• Lay understanding of genetic disease: A British study of families attending a genetic counseling service
  Journal of Genetic Counseling, 1995
• The contribution of the DFNB1 locus to neurosensory deafness in a Caucasian population.
  1995
• Prenatal screening for cystic fibrosis: attitudes and responses of participants
  Clinical Genetics, 1993
• Cystic fibrosis: community knowledge and attitudes towards carrier screening and prenatal diagnosis
  Clinical Genetics, 1992
• Recurrence Risks
  Annals of the New York Academy of Sciences, 1991
• Community attitudes to cystic fibrosis carrier testing in England: A pilot study
  Prenatal Diagnosis, 1989
• Stigmatization of carrier status: social implications of heterozygote genetic screening programs.
  American Journal of Public Health, 1978