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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

172 related items for PubMed ID: 20488870

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  • 3. A prospective, longitudinal study of the impact of GJB2/GJB6 genetic testing on the beliefs and attitudes of parents of deaf and hard-of-hearing infants.
    Palmer CG, Martinez A, Fox M, Zhou J, Shapiro N, Sininger Y, Grody WW, Schimmenti LA.
    Am J Med Genet A; 2009 Jun; 149A(6):1169-82. PubMed ID: 19449415
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  • 4. The genetics of deafness.
    Nance WE.
    Ment Retard Dev Disabil Res Rev; 2003 Jun; 9(2):109-19. PubMed ID: 12784229
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  • 6. Impact of genetic advances and testing for hearing loss: results from a national consumer survey.
    Withrow KA, Tracy KA, Burton SK, Norris VW, Maes HH, Arnos KS, Pandya A.
    Am J Med Genet A; 2009 Jun; 149A(6):1159-68. PubMed ID: 19449400
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  • 7. Attitudes of deaf adults toward genetic testing for hereditary deafness.
    Middleton A, Hewison J, Mueller RF.
    Am J Hum Genet; 1998 Oct; 63(4):1175-80. PubMed ID: 9758618
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  • 9. Genetic selection for deafness: the views of hearing children of deaf adults.
    Mand C, Duncan RE, Gillam L, Collins V, Delatycki MB.
    J Med Ethics; 2009 Dec; 35(12):722-8. PubMed ID: 19948926
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  • 13. Factors influencing parental decision about genetics evaluation for their deaf or hard-of-hearing child.
    Palmer CG, Lueddeke JT, Zhou J.
    Genet Med; 2009 Apr; 11(4):248-55. PubMed ID: 19265722
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  • 14. Frequency and distribution of GJB2 (connexin 26) and GJB6 (connexin 30) mutations in a large North American repository of deaf probands.
    Pandya A, Arnos KS, Xia XJ, Welch KO, Blanton SH, Friedman TB, Garcia Sanchez G, Liu MD XZ, Morell R, Nance WE.
    Genet Med; 2003 Apr; 5(4):295-303. PubMed ID: 12865758
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  • 17. Frequency of the 35delG mutation in the connexin 26 gene in Turkish hearing-impaired patients.
    Bariş I, Kilinç MO, Tolun A.
    Clin Genet; 2001 Dec; 60(6):452-5. PubMed ID: 11846738
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