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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

169 related items for PubMed ID: 19265722

  • 1.
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  • 2. 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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  • 3. 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 Jun; 5(4):295-303. PubMed ID: 12865758
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  • 5. Does universal newborn hearing screening identify all children with GJB2 (Connexin 26) deafness? Penetrance of GJB2 deafness.
    Norris VW, Arnos KS, Hanks WD, Xia X, Nance WE, Pandya A.
    Ear Hear; 2006 Dec; 27(6):732-41. PubMed ID: 17086082
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  • 8. 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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  • 9. 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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  • 13. [Prenatal diagnosis for hereditary deaf families assisted by genetic testing].
    Han B, Dai P, Qi QW, Wang LX, Wang Y, Bian XM, Wang QJ, Zhang X, Kang DY, Wang GJ, Han DY.
    Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2007 Sep; 42(9):660-3. PubMed ID: 18051563
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  • 15. 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. PubMed ID: 17542005
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  • 16. Screening for monogenetic del(GJB6-D13S1830) and digenic del(GJB6-D13S1830)/GJB2 patterns of inheritance in deaf individuals from Eastern Austria.
    Frei K, Ramsebner R, Lucas T, Baumgartner WD, Schoefer C, Wachtler FJ, Kirschhofer K.
    Hear Res; 2004 Oct 15; 196(1-2):115-8. PubMed ID: 15464308
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  • 17. Parental attitudes toward genetic testing for prelingual deafness in China.
    Fu S, Dong J, Wang C, Chen G.
    Int J Pediatr Otorhinolaryngol; 2010 Oct 15; 74(10):1122-5. PubMed ID: 20637511
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  • 18. Hearing Loss: Genetic Testing, Current Advances and the Situation in Latin America.
    De Rosa MA, Bernardi MT, Kleppe S, Walz K.
    Genes (Basel); 2024 Jan 29; 15(2):. PubMed ID: 38397168
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  • 19. [Prenatal genetic test and clinical guidance for 213 hereditary deaf families].
    Han MY, Lu YP, Bian XM, Wang LX, Huang SS, Wang GJ, Wang Y, Kang DY, Zhang X, Dai P.
    Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2012 Feb 29; 47(2):127-31. PubMed ID: 22455811
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  • 20. Deaf adults' reasons for genetic testing depend on cultural affiliation: results from a prospective, longitudinal genetic counseling and testing study.
    Boudreault P, Baldwin EE, Fox M, Dutton L, Tullis L, Linden J, Kobayashi Y, Zhou J, Sinsheimer JS, Sininger Y, Grody WW, Palmer CG.
    J Deaf Stud Deaf Educ; 2010 Feb 29; 15(3):209-27. PubMed ID: 20488870
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