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Results: 1 to 20 of 104

1.

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

Etchegary H, Dicks E, Green J, Hodgkinson K, Pullman D, Parfrey P.

Genet Test Mol Biomarkers. 2012 May;16(5):353-8. doi: 10.1089/gtmb.2011.0221. Epub 2011 Nov 21.

PMID:
22103558
[PubMed - indexed for MEDLINE]
2.

Public attitudes about genetic testing in the newborn period.

Etchegary H, Dicks E, Hodgkinson K, Pullman D, Green J, Parfey P.

J Obstet Gynecol Neonatal Nurs. 2012 Mar;41(2):191-200. doi: 10.1111/j.1552-6909.2012.01341.x.

PMID:
22834846
[PubMed - indexed for MEDLINE]
3.

Attitudes of genetic counselors towards expanding newborn screening and offering predictive genetic testing to children.

Hiraki S, Ormond KE, Kim K, Ross LF.

Am J Med Genet A. 2006 Nov 1;140(21):2312-9.

PMID:
17036312
[PubMed - indexed for MEDLINE]
4.

[Attitudes towards prenatal diagnosis of deafness among parents to children with cochlear implants].

Thorsen A, Devantier L, Ovesen T.

Ugeskr Laeger. 2009 Apr 20;171(17):1387-91. Danish.

PMID:
19413935
[PubMed - indexed for MEDLINE]
5.

Pediatricians' attitudes toward expanding newborn screening.

Acharya K, Ackerman PD, Ross LF.

Pediatrics. 2005 Oct;116(4):e476-84.

PMID:
16199673
[PubMed - indexed for MEDLINE]
Free Article
6.

Neonatal screening for treatable and untreatable disorders: prospective parents' opinions.

Plass AM, van El CG, Pieters T, Cornel MC.

Pediatrics. 2010 Jan;125(1):e99-106. doi: 10.1542/peds.2009-0269. Epub 2009 Dec 21.

PMID:
20026497
[PubMed - indexed for MEDLINE]
Free Article
7.

A focus group study of consumer attitudes toward genetic testing and newborn screening for deafness.

Burton SK, Withrow K, Arnos KS, Kalfoglou AL, Pandya A.

Genet Med. 2006 Dec;8(12):779-83.

PMID:
17172941
[PubMed - indexed for MEDLINE]
8.

Parental attitudes toward ethical and social issues surrounding the expansion of newborn screening using new technologies.

Hasegawa LE, Fergus KA, Ojeda N, Au SM.

Public Health Genomics. 2011;14(4-5):298-306. doi: 10.1159/000314644. Epub 2010 Jul 30.

PMID:
20689248
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Parental narratives on genetic testing for children with hearing loss: a qualitative inquiry.

Steinberg AG, Kaimal G, Bain L, Krantz I, Li Y.

Am J Med Genet A. 2007 Jul 15;143A(14):1533-45.

PMID:
17542005
[PubMed - indexed for MEDLINE]
10.

Consent for newborn screening: the attitudes of health care providers.

Miller FA, Hayeems RZ, Carroll JC, Wilson B, Little J, Allanson J, Bytautas JP, Paynter M, Christensen R, Chaktraborty P.

Public Health Genomics. 2010;13(3):181-90. doi: 10.1159/000240966. Epub 2009 Sep 22.

PMID:
19776551
[PubMed - indexed for MEDLINE]
11.

Genetic testing for hearing loss: different motivations for the same outcome.

Dagan O, Hochner H, Levi H, Raas-Rothschild A, Sagi M.

Am J Med Genet. 2002 Nov 22;113(2):137-43.

PMID:
12407703
[PubMed - indexed for MEDLINE]
12.

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

Ciske DJ, Haavisto A, Laxova A, Rock LZ, Farrell PM.

Pediatrics. 2001 Apr;107(4):699-705.

PMID:
11335747
[PubMed - indexed for MEDLINE]
13.

Parental attitudes to the identification of their infants as carriers of cystic fibrosis by newborn screening.

Lewis S, Curnow L, Ross M, Massie J.

J Paediatr Child Health. 2006 Sep;42(9):533-7.

PMID:
16925540
[PubMed - indexed for MEDLINE]
14.

Early hearing detection and intervention: parent experiences with the diagnostic hearing assessment.

Larsen R, Muñoz K, DesGeorges J, Nelson L, Kennedy S.

Am J Audiol. 2012 Jun;21(1):91-9. doi: 10.1044/1059-0889(2012/11-0016). Epub 2012 Mar 26.

PMID:
22451071
[PubMed - indexed for MEDLINE]
15.

Screening for Fragile X Syndrome: parent attitudes and perspectives.

Skinner D, Sparkman KL, Bailey DB Jr.

Genet Med. 2003 Sep-Oct;5(5):378-84.

PMID:
14501833
[PubMed - indexed for MEDLINE]
16.

Maternal attitudes to newborn screening for fragile X syndrome.

Christie L, Wotton T, Bennetts B, Wiley V, Wilcken B, Rogers C, Boyle J, Turner C, Hansen J, Hunter M, Goel H, Field M.

Am J Med Genet A. 2013 Feb;161A(2):301-11. doi: 10.1002/ajmg.a.35752. Epub 2013 Jan 9.

PMID:
23303663
[PubMed - indexed for MEDLINE]
17.

Parents' decision-making in newborn screening: opinions, choices, and information needs.

Lipstein EA, Nabi E, Perrin JM, Luff D, Browning MF, Kuhlthau KA.

Pediatrics. 2010 Oct;126(4):696-704. doi: 10.1542/peds.2010-0217. Epub 2010 Sep 13.

PMID:
20837593
[PubMed - indexed for MEDLINE]
Free Article
18.

Informing parents about newborn screening.

Kemper AR, Fant KE, Clark SJ.

Public Health Nurs. 2005 Jul-Aug;22(4):332-8.

PMID:
16150014
[PubMed - indexed for MEDLINE]
19.

Parental attitudes regarding newborn screening of PKU and DMD.

Campbell E, Ross LF.

Am J Med Genet A. 2003 Jul 15;120A(2):209-14.

PMID:
12833401
[PubMed - indexed for MEDLINE]
20.

Attitudes of families affected by adrenoleukodystrophy toward prenatal diagnosis, presymptomatic and carrier testing, and newborn screening.

Schaller J, Moser H, Begleiter ML, Edwards J.

Genet Test. 2007 Fall;11(3):296-302.

PMID:
17949291
[PubMed - indexed for MEDLINE]

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