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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

312 related items for PubMed ID: 15699983

  • 21.
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  • 22. On the etiology of hearing loss in a population of 155 institutionalized children.
    Dereymaeker AM, Fryns JP, Ars B, Andrescescou J, Van den Berghe H.
    Acta Otorhinolaryngol Belg; 1991; 45(3):283-91. PubMed ID: 1659109
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  • 23.
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  • 25. [Mode of inheritance of congenital deaf-mutism].
    Hu DN, Qiu WQ, Wu BT, Fang LZ, Zhou F, Gu YP, Zhang QH, Yan JH.
    Yi Chuan Xue Bao; 1988; 15(4):303-8. PubMed ID: 3273676
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  • 26. Cochlear alterations in deaf and unaffected subjects carrying the deafness-associated A1555G mutation in the mitochondrial 12S rRNA gene.
    Bravo O, Ballana E, Estivill X.
    Biochem Biophys Res Commun; 2006 Jun 02; 344(2):511-6. PubMed ID: 16631122
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  • 27. Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA mutation in 16 Chinese families: implication for early detection and prevention of deafness.
    Dai P, Liu X, Han D, Qian Y, Huang D, Yuan H, Li W, Yu F, Zhang R, Lin H, He Y, Yu Y, Sun Q, Qin H, Li R, Zhang X, Kang D, Cao J, Young WY, Guan MX.
    Biochem Biophys Res Commun; 2006 Feb 03; 340(1):194-9. PubMed ID: 16375862
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  • 29. [Hearing and speech therapeutical services to the population of the Moscow region (contribution of Prof. M. A. Shuster in its organization].
    Sambulov VI, Chkannikov AN, Kokoreva SA, Torbochkina NN, Kolesnikova TA, Mkhaĭmar N.
    Vestn Otorinolaringol; 2002 Feb 03; (3):50-2. PubMed ID: 12227033
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  • 32. [Medico-genetic study of the population of Kostroma Province. I. The population burden of hereditary pathology].
    Ginter EK, Revazov AA, Talanov MI, Nechvolodova OL, Khlebnikova OV.
    Genetika; 1985 Jan 03; 21(1):153-60. PubMed ID: 3156065
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  • 36. Prevalence, heritability and genetic correlations of congenital sensorineural deafness and pigmentation phenotypes in the Border Collie.
    De Risio L, Lewis T, Freeman J, de Stefani A, Matiasek L, Blott S.
    Vet J; 2011 Jun 03; 188(3):286-90. PubMed ID: 20570536
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  • 37. Congenital cochlear deafness in mitochondrial diseases related to RRM2B and SERAC1 gene defects. A study of the mitochondrial patients of the CMHI hospital in Warsaw, Poland.
    Iwanicka-Pronicka K, Ciara E, Piekutowska-Abramczuk D, Halat P, Pajdowska M, Pronicki M.
    Int J Pediatr Otorhinolaryngol; 2019 Jun 03; 121():143-149. PubMed ID: 30909120
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  • 38. An epidemiological study of hearing loss in a slum in Pune.
    Dutta PK, Banerjee A.
    Indian J Public Health; 1991 Jun 03; 35(4):108-12. PubMed ID: 1821882
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  • 39. [Importance of audiological examinations of hearing parents of children with congenital hearing defects of undetermined origin].
    Courtoy M, Hennebert D, Perier O, Van den Haute J.
    Acta Otorhinolaryngol Belg; 1972 Jun 03; 26(6):629-34. PubMed ID: 4669676
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  • 40. Epidemiological study of mumps deafness in Japan.
    Kawashima Y, Ihara K, Nakamura M, Nakashima T, Fukuda S, Kitamura K.
    Auris Nasus Larynx; 2005 Jun 03; 32(2):125-8. PubMed ID: 15917168
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