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

182 related items for PubMed ID: 9238477

  • 1. [A case of Waardenburg-Klein syndrome observed at the Cotonou NUHC].
    Bassabi SK, Medji AP, Doutetien C, Oussa G, Hounkpe YY, Vodouhe SJ, Babagbeto M, Latoundji S.
    J Fr Ophtalmol; 1997; 20(5):387-90. PubMed ID: 9238477
    [Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3. [Waardenburg syndrome type I--autosomal dominant hereditary combination of multiple facial anomalies with cochlear deafness (author's transl)].
    Meinecke P.
    Klin Padiatr; 1982 Mar; 194(2):112-6. PubMed ID: 7098370
    [Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5. Autosomal dominant inheritance of Klein-Waardenburg syndrome.
    Sheffer R, Zlotogora J.
    Am J Med Genet; 1992 Feb 01; 42(3):320-2. PubMed ID: 1536170
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. Waardenburg syndrome type II: phenotypic findings and diagnostic criteria.
    Liu XZ, Newton VE, Read AP.
    Am J Med Genet; 1995 Jan 02; 55(1):95-100. PubMed ID: 7702105
    [Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. [Waardenburg-Klein syndrome. Description of 2 cases].
    Fregonese B, Vignola G, Mori PG, Grossi Bianchi ML.
    Minerva Pediatr; 1969 Aug 18; 21(33):1513-9. PubMed ID: 5361984
    [No Abstract] [Full Text] [Related]

  • 17. Genetic heterogeneity in the Waardenburg syndrome.
    Arias S.
    Birth Defects Orig Artic Ser; 1971 Mar 18; 07(4):87-101. PubMed ID: 5006208
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. [Hereditary unilateral deaf-mutism as a variable manifestation of bilateral deaf-mutism or hearing loss].
    Graf K.
    Laryngorhinootologie; 1992 May 18; 71(5):242-5. PubMed ID: 1616543
    [Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 10.