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

176 related items for PubMed ID: 2248288

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. GAPO syndrome: report of three affected brothers.
    Gagliardi AR, González CH, Pratesi R.
    Am J Med Genet; 1984 Oct; 19(2):217-23. PubMed ID: 6507472
    [Abstract] [Full Text] [Related]

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

  • 8. [Ocular manifestation in GAPO syndrome. Report of the first tunisian case].
    Touzri RA, Goucha S, Kriaa L, Beltaif O, Fazaa B, El Andolsi H, Kamoun MR, Ouertani A.
    J Fr Ophtalmol; 2003 Dec; 26(10):1067-70. PubMed ID: 14691402
    [Abstract] [Full Text] [Related]

  • 9. [Ophthalmological anomalies of the GAPO syndrome (growth retardation, alopecia, pseudo-anodontia, optic atrophy). Apropos of a case].
    Dellac M, Manouvrier-Hanu S, Rouland JF.
    J Fr Ophtalmol; 1990 Dec; 13(11-12):547-50. PubMed ID: 2081845
    [Abstract] [Full Text] [Related]

  • 10. Ophthalmic findings in GAPO syndrome.
    Ilker SS, Oztürk F, Kurt E, Temel M, Gül D, Sayli BS.
    Jpn J Ophthalmol; 1999 Dec; 43(1):48-52. PubMed ID: 10197743
    [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. GAPO syndrome: a new case of this rare syndrome and a review of the relative importance of different phenotypic features in diagnosis.
    Bacon W, Hall RK, Roset JP, Boukari A, Tenenbaum H, Walter B.
    J Craniofac Genet Dev Biol; 1999 Dec; 19(4):189-200. PubMed ID: 10731088
    [Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. A new syndrome of dwarfism, brachydactyly, nail dysplasia, and mental retardation in sibs.
    Tonoki H, Kishino T, Niikawa N.
    Am J Med Genet; 1990 May; 36(1):89-93. PubMed ID: 2333912
    [Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. GAPO syndrome: three new Brazilian cases, additional osseous manifestations, and review of the literature.
    Goloni-Bertollo EM, Ruiz MT, Goloni CB, Muniz MP, Valério NI, Pavarino-Bertelli EC.
    Am J Med Genet A; 2008 Jun 15; 146A(12):1523-9. PubMed ID: 18470892
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 9.