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Volumn 16, Issue 5, 2012, Pages 353-358

Interest in newborn genetic testing: A survey of prospective parents and the general public

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CROSS-SECTIONAL STUDY; FEMALE; HEARING LOSS; HUMAN; MAJOR CLINICAL STUDY; MALE; NEUROLOGIC DISEASE; NEWBORN; NEWBORN SCREENING; PARENT; PARENTAL ATTITUDE; STUDENT; VISUAL IMPAIRMENT;

EID: 84861496136     PISSN: 19450265     EISSN: 19450257     Source Type: Journal    
DOI: 10.1089/gtmb.2011.0221     Document Type: Article
Times cited : (15)

References (15)
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  • 2
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  • 3
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    • Brunger J, Murray G, O'Riordan M, et al. (2000) Parental attitudes toward genetic testing for pediatric deafness. Am J Hum Genet 67:1621-1625.
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  • 4
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    • Canadian Organization for Rare Disorders accessed November 16 2010
    • Canadian Organization for Rare Disorders (2010) Newborn screening in Canada status report. Available at http://raredisorders.ca/documents/ CanadaNBSstatusupdatedNov .112010.pdf, accessed November 16, 2010.
    • (2010) Newborn Screening in Canada Status Report
  • 5
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  • 6
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    • (2011) Public Health Genomics , vol.14 , pp. 298-306
    • Hasegawa, L.1    Fergus, K.2    Ojeda, N.3
  • 7
    • 77957703237 scopus 로고    scopus 로고
    • Parents' decision-making in newborn screening: Opinions, choices and information needs
    • Lipstein E, Nabi E, Perrin J, et al. (2010) Parents' decision-making in newborn screening: opinions, choices and information needs. Pediatrics 126:696-704.
    • (2010) Pediatrics , vol.126 , pp. 696-704
    • Lipstein, E.1    Nabi, E.2    Perrin, J.3
  • 8
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    • Expanding newborn screening: Process, policy and priorities
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  • 9
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  • 10
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  • 15
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.