These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

97 related items for PubMed ID: 10051011

  • 41.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 42. Cancer families: what risks are they given and do the risks affect management?
    Rosser EM, Hurst JA, Chapman CJ.
    J Med Genet; 1996 Dec; 33(12):977-80. PubMed ID: 9004126
    [Abstract] [Full Text] [Related]

  • 43.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 44. Recurrence risks.
    Smith SD.
    Ann N Y Acad Sci; 1991 Dec; 630():203-11. PubMed ID: 1952591
    [No Abstract] [Full Text] [Related]

  • 45. Prelingual deafness.
    Keith WJ, Senanayake SM.
    N Z Med J; 1984 Feb 08; 97(749):91-2. PubMed ID: 6583573
    [No Abstract] [Full Text] [Related]

  • 46.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 47.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 48.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 49.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 50.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 51.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 52. [Special practical problems in deafness in childhood].
    OMBREDANNE M.
    Vie Med; 1961 Feb 08; 42():1035-40. PubMed ID: 13730941
    [No Abstract] [Full Text] [Related]

  • 53.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 54. Common genes for non-syndromic deafness are uncommon in sub-Saharan Africa: a report from Nigeria.
    Lasisi AO, Bademci G, Foster J, Blanton S, Tekin M.
    Int J Pediatr Otorhinolaryngol; 2014 Nov 08; 78(11):1870-3. PubMed ID: 25218342
    [Abstract] [Full Text] [Related]

  • 55. Deafness in children: a national survey of aetiological investigations.
    Rangan S, Borgstein B, Lowe J.
    BMJ Open; 2012 Nov 08; 2(5):. PubMed ID: 22983783
    [Abstract] [Full Text] [Related]

  • 56.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 57.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 58. [Etiological diagnosis of sensorineural deafness in children: a year-long review of genetic counseling for deaf people].
    Marlin S, Denoyelle F, Garabédian EN, Petit C.
    Ann Otolaryngol Chir Cervicofac; 1998 Feb 08; 115(1):3-8. PubMed ID: 9765703
    [Abstract] [Full Text] [Related]

  • 59.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 60. [Organization of medico-genetic counseling for hereditary hearing impairment].
    Markova TG.
    Vestn Otorinolaringol; 2009 Feb 08; (1):34-6. PubMed ID: 19365361
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 5.