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Journal Abstract Search

74 related items for PubMed ID: 3091213

  • 1. [Analysis of 223 cases of hereditary deafness].
    Zhuang JM, Wang DX.
    Zhonghua Yi Xue Za Zhi; 1986 Jan; 66(1):25-8. PubMed ID: 3091213
    [No Abstract] [Full Text] [Related]

  • 2. [Do hemoglobinopathies correlate with genetically-induced hearing disorders?].
    Radü HJ.
    Laryngol Rhinol Otol (Stuttg); 1985 Sep; 64(9):473-5. PubMed ID: 2417080
    [Abstract] [Full Text] [Related]

  • 3. [Clinical and genetical analysis of a family with hereditary congenital conductive hearing loss and proximal symphalangism and amblyopia].
    Luo HJ, Jin XJ, Shi WR.
    Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2006 Apr; 41(4):310-1. PubMed ID: 16848189
    [No Abstract] [Full Text] [Related]

  • 4. Conductive deafness with ptosis and skeletal malformations in sibs: a probably autosomal recessive disorder.
    Jackson LG, Barr MA.
    Birth Defects Orig Artic Ser; 1978 Apr; 14(6B):199-204. PubMed ID: 728561
    [No Abstract] [Full Text] [Related]

  • 5. [Hereditary progressive sensorineural deafness--report of 30 cases in 12 families].
    Wang X.
    Zhonghua Yi Xue Za Zhi; 1983 Nov; 63(11):694-8. PubMed ID: 6426737
    [No Abstract] [Full Text] [Related]

  • 6. 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
    [Abstract] [Full Text] [Related]

  • 7. Hereditary hearing loss associated with musculoskeletal malformations.
    Gorlin RJ.
    Birth Defects Orig Artic Ser; 1980 Feb 03; 16(7):73-87. PubMed ID: 6260264
    [No Abstract] [Full Text] [Related]

  • 8. A distinct dominant form of microtia and conductive hearing loss.
    Sánchez-Corona J, García-Cruz D, Ruenes R, Cantú JM.
    Birth Defects Orig Artic Ser; 1982 Feb 03; 18(3B):211-6. PubMed ID: 7139104
    [No Abstract] [Full Text] [Related]

  • 9. Conductive deafness, symphalangism, and facial abnormalities: the WL syndrome in a Japanese family.
    Higashi K, Inoue S.
    Am J Med Genet; 1983 Sep 03; 16(1):105-9. PubMed ID: 6638061
    [Abstract] [Full Text] [Related]

  • 10. [Hereditary nephritis with deafness in one family].
    Golev GD.
    Klin Med (Mosk); 1989 Nov 03; 67(11):128-30. PubMed ID: 2625948
    [No Abstract] [Full Text] [Related]

  • 11. [HLA-antigens and sensorineural deafness].
    Gross M, Arndt-Hanser A.
    Laryngol Rhinol Otol (Stuttg); 1982 Jun 03; 61(6):316-8. PubMed ID: 7121151
    [Abstract] [Full Text] [Related]

  • 12. Familial microtia in four generations with variable expressivity and incomplete penetrance in association with type I syndactyly.
    Balci S, Boduroğlu K, Kaya S.
    Turk J Pediatr; 2001 Jun 03; 43(4):362-5. PubMed ID: 11765172
    [Abstract] [Full Text] [Related]

  • 13. Alport's syndrome of hereditary nephritis and deafness.
    Crawfurd MD, Toghill PJ.
    Q J Med; 1968 Oct 03; 37(148):563-76. PubMed ID: 5696367
    [No Abstract] [Full Text] [Related]

  • 14. Familial microtia with meatal atresia and conductive deafness in five generations.
    Gupta A, Patton MA.
    Am J Med Genet; 1995 Nov 06; 59(2):238-41. PubMed ID: 8588593
    [Abstract] [Full Text] [Related]

  • 15. Dominantly inherited low-frequency hearing loss.
    Arch Otolaryngol; 1968 Sep 06; 88(3):242-50. PubMed ID: 5663381
    [No Abstract] [Full Text] [Related]

  • 16. [Non-syndromic familial deafness. Review and genetic study].
    Guiral H, Flores JC, Risco J, Figuerola E, Pellicer F.
    Acta Otorrinolaringol Esp; 1996 Sep 06; 47(4):272-6. PubMed ID: 8962727
    [Abstract] [Full Text] [Related]

  • 17. Frequency of the branchio-oto-renal (BOR) syndrome in children with profound hearing loss.
    Fraser FC, Sproule JR, Halal F.
    Am J Med Genet; 1980 Sep 06; 7(3):341-9. PubMed ID: 7468659
    [Abstract] [Full Text] [Related]

  • 18. Familial low frequency hearing loss.
    Konigsmark BW, Mengel M, Berlin CI.
    Laryngoscope; 1971 May 06; 81(5):759-71. PubMed ID: 5157378
    [No Abstract] [Full Text] [Related]

  • 19. Mitochondrial A7445G mutation in two pedigrees with palmoplantar keratoderma and deafness.
    Sevior KB, Hatamochi A, Stewart IA, Bykhovskaya Y, Allen-Powell DR, Fischel-Ghodsian N, Maw MA.
    Am J Med Genet; 1998 Jan 13; 75(2):179-85. PubMed ID: 9450881
    [Abstract] [Full Text] [Related]

  • 20. Mouse models to study inner ear development and hereditary hearing loss.
    Friedman LM, Dror AA, Avraham KB.
    Int J Dev Biol; 2007 Jan 13; 51(6-7):609-31. PubMed ID: 17891721
    [Abstract] [Full Text] [Related]

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