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Journal Abstract Search

169 related items for PubMed ID: 19265722

  • 21. The use of genetic testing in the evaluation of hearing impairment in a child.
    Robin NH, Prucka SK, Woolley AL, Smith RJ.
    Curr Opin Pediatr; 2005 Dec; 17(6):709-12. PubMed ID: 16282775
    [Abstract] [Full Text] [Related]

  • 22. [Prenatal genetic counseling and instruction for deaf families by genetic test].
    Han MY, Huang SS, Wang GJ, Yuan YY, Kang DY, Zhang X, Dai P.
    Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2011 Nov; 46(11):909-13. PubMed ID: 22335977
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  • 24. Molecular genetics study of deafness in Brazil: 8-year experience.
    de Oliveira CA, Alexandrino F, Christiani TV, Steiner CE, Cunha JL, Guerra AT, Sartorato EL.
    Am J Med Genet A; 2007 Jul 15; 143A(14):1574-9. PubMed ID: 17567887
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  • 25. Role of GJB2 and GJB6 in Iranian Nonsyndromic Hearing Impairment: From Molecular Analysis to Literature Reviews.
    Falah M, Houshmand M, Balali M, Asghari A, Bagher Z, Alizadeh R, Farhadi M.
    Fetal Pediatr Pathol; 2020 Feb 15; 39(1):1-12. PubMed ID: 31215297
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  • 26. Prevalence of GJB2 (connexin-26) and GJB6 (connexin-30) mutations in a cohort of 300 Brazilian hearing-impaired individuals: implications for diagnosis and genetic counseling.
    Batissoco AC, Abreu-Silva RS, Braga MC, Lezirovitz K, Della-Rosa V, Alfredo T, Otto PA, Mingroni-Netto RC.
    Ear Hear; 2009 Feb 15; 30(1):1-7. PubMed ID: 19125024
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  • 27. Sharing GJB2/GJB6 genetic test information with family members.
    Blase T, Martinez A, Grody WW, Schimmenti L, Palmer CG.
    J Genet Couns; 2007 Jun 15; 16(3):313-24. PubMed ID: 17318457
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  • 29. Connexin 26 variants and auditory neuropathy/dys-synchrony among children in schools for the deaf.
    Cheng X, Li L, Brashears S, Morlet T, Ng SS, Berlin C, Hood L, Keats B.
    Am J Med Genet A; 2005 Nov 15; 139(1):13-8. PubMed ID: 16222667
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  • 31. Perception of Genetic Testing for Deafness and Factors Associated with Interest in Genetic Testing Among Deaf People in a Selected Population in Sub-Saharan Africa.
    Adedokun BO, Yusuf BO, Lasisi JT, Jinadu AA, Sunmonu MT, Ashanke AF, Lasisi OA.
    J Genet Couns; 2015 Dec 15; 24(6):1037-43. PubMed ID: 25983050
    [Abstract] [Full Text] [Related]

  • 32. Early identification: Language skills and social functioning in deaf and hard of hearing preschool children.
    Netten AP, Rieffe C, Theunissen SC, Soede W, Dirks E, Korver AM, Konings S, Oudesluys-Murphy AM, Dekker FW, Frijns JH, DECIBEL Collaborative study group.
    Int J Pediatr Otorhinolaryngol; 2015 Dec 15; 79(12):2221-6. PubMed ID: 26514930
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  • 33. Consumer motivations for pursuing genetic testing and their preferences for the provision of genetic services for hearing loss.
    Withrow KA, Burton S, Arnos KS, Kalfoglou A, Pandya A.
    J Genet Couns; 2008 Jun 15; 17(3):252-60. PubMed ID: 18247107
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  • 34. 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 15; 35(12):722-8. PubMed ID: 19948926
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  • 35. Molecular studies in the GJB2 gene (Cx26) among a deaf population from Bogotá, Colombia: results of a screening program.
    Tamayo ML, Olarte M, Gelvez N, Gómez M, Frías JL, Bernal JE, Florez S, Medina D.
    Int J Pediatr Otorhinolaryngol; 2009 Jan 15; 73(1):97-101. PubMed ID: 19027181
    [Abstract] [Full Text] [Related]

  • 36. Role of DFNB1 mutations in hereditary hearing loss among assortative mating hearing impaired families from South India.
    Amritkumar P, Jeffrey JM, Chandru J, Vanniya S P, Kalaimathi M, Ramakrishnan R, Karthikeyen NP, Srikumari Srisailapathy CR.
    BMC Med Genet; 2018 Jun 19; 19(1):105. PubMed ID: 29921236
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  • 37. Clinical evaluation and etiologic diagnosis of hearing loss: A clinical practice resource of the American College of Medical Genetics and Genomics (ACMG).
    Li MM, Tayoun AA, DiStefano M, Pandya A, Rehm HL, Robin NH, Schaefer AM, Yoshinaga-Itano C, ACMG Professional Practice and Guidelines Committee. Electronic address: documents@acmg.netAmerican College of Medical Genetics and Genomics, Bethesda, MD..
    Genet Med; 2022 Jul 19; 24(7):1392-1406. PubMed ID: 35802133
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  • 38. Etiology and associated GJB2 mutations in Mauritanian children with non-syndromic hearing loss.
    Moctar EC, Riahi Z, El Hachmi H, Veten F, Meiloud G, Bonnet C, Abdelhak S, Errami M, Houmeida A.
    Eur Arch Otorhinolaryngol; 2016 Nov 19; 273(11):3693-3698. PubMed ID: 27067584
    [Abstract] [Full Text] [Related]

  • 39. Attitudes of deaf and hard of hearing subjects towards genetic testing and prenatal diagnosis of hearing loss.
    Stern SJ, Arnos KS, Murrelle L, Welch KO, Nance WE, Pandya A.
    J Med Genet; 2002 Jun 19; 39(6):449-53. PubMed ID: 12070258
    [No Abstract] [Full Text] [Related]

  • 40. Effect of pre-test genetic counseling for deaf adults on knowledge of genetic testing.
    Baldwin EE, Boudreault P, Fox M, Sinsheimer JS, Palmer CG.
    J Genet Couns; 2012 Apr 19; 21(2):256-72. PubMed ID: 21818696
    [Abstract] [Full Text] [Related]

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